Canonical Allele Identifier:
CA120582
Gene:
Linked Data
ClinVar Variation Id:
9619
ClinVar RCV Id:
RCV000010244
dbSNP Id:
rs121434454
MyVariant Identifiers:
chrMT:g.7526A>G (hg38)
PubMed:
PMID:16059939
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.7526A>G , J01415.2:m.7526A>G | GRCh38 |