Canonical Allele Identifier:
CA120586
Gene:
Identifiers and link-outs to other resources
ClinVar Variation Id:
9623
ClinVar RCV Id:
RCV000010249
dbSNP Id:
rs121434456
MyVariant Identifiers:
chrMT:g.10438A>G (hg38)
User contributed link-outs
PubMed:
PMID:15286228
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.10438A>G , J01415.2:m.10438A>G | GRCh38 |