Canonical Allele Identifier:
CA120540
Gene:
Linked Data
ClinVar Variation Id:
9554
ClinVar RCV Id:
RCV000010163
dbSNP Id:
rs199474671
MyVariant Identifiers:
chrMT:g.5549G>A (hg38)
PubMed:
PMID:7695240
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_012920.1:m.5549G>A , J01415.2:m.5549G>A | GRCh38 |