{
  "description": "HGVS nomenclature is used to report and exchange information regarding variants found in DNA, RNA, and protein sequences.",
  "compose": {
    "include": [ {
      "system": "http://varnomen.hgvs.org"
    } ]
  },
  "_filename": "ValueSet-mcode-hgvs-vs.json",
  "package_name": "hl7.fhir.us.mcode",
  "date": "2022-01-18T03:17:40+00:00",
  "publisher": "HL7 International Clinical Interoperability Council",
  "jurisdiction": [ {
    "coding": [ {
      "code": "US",
      "system": "urn:iso:std:iso:3166",
      "display": "United States of America"
    } ]
  } ],
  "name": "HGVSVS",
  "type": null,
  "experimental": null,
  "resourceType": "ValueSet",
  "title": "Human Genome Variation Society Sequence Variant Nomenclature Value Set",
  "package_version": "2.0.0",
  "status": "active",
  "id": "3757dcc3-747a-4faa-8eb9-8c1bf60f291f",
  "kind": null,
  "url": "http://hl7.org/fhir/us/mcode/ValueSet/mcode-hgvs-vs",
  "version": "2.0.0",
  "contact": [ {
    "name": "HL7 International Clinical Interoperability Council",
    "telecom": [ {
      "value": "http://www.hl7.org/Special/committees/cic",
      "system": "url"
    }, {
      "value": "ciclist@lists.HL7.org",
      "system": "email"
    } ]
  } ]
}