Canonical Allele Identifier: CA254846
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 9630
dbSNP Id: rs267606620
MyVariant Identifiers: chrMT:g.1291T>C (hg38)

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1291T>C , J01415.2:m.1291T>C GRCh38