Canonical Allele Identifier:
CA120573
Gene:
Linked Data
ClinVar Variation Id:
9607
ClinVar RCV Id:
RCV000010230
dbSNP Id:
rs121434471
MyVariant Identifiers:
chrMT:g.4291T>C (hg38)
PubMed:
PMID:15498972
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.4291T>C , J01415.2:m.4291T>C | GRCh38 |