Canonical Allele Identifier:
CA337100625
Gene:
Linked Data
ClinVar Variation Id:
690275
ClinVar RCV Id:
RCV000851173
dbSNP Id:
rs201864830
MyVariant Identifiers:
chrMT:g.16017T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.16017T>C , J01415.2:m.16017T>C | GRCh38 |