Canonical Allele Identifier:
CA120575
Gene:
Linked Data
ClinVar Variation Id:
9609
ClinVar RCV Id:
RCV000010233
dbSNP Id:
rs121434473
MyVariant Identifiers:
chrMT:g.12183G>A (hg38)
PubMed:
PMID:12682337
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.12183G>A , J01415.2:m.12183G>A | GRCh38 |