Canonical Allele Identifier:
CA120589
Gene:
Linked Data
ClinVar Variation Id:
9627
ClinVar RCV Id:
RCV000010253
dbSNP Id:
rs199474824
MyVariant Identifiers:
chrMT:g.2939C>A (hg38)
PubMed:
PMID:6273808
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.2939C>A , J01415.2:m.2939C>A | GRCh38 |