Canonical Allele Identifier: CA120601
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 9655
ClinVar RCV Id: RCV000010291
dbSNP Id: rs267606613
MyVariant Identifiers: chrMT:g.9952G>A (hg38)

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9952G>A , J01415.2:m.9952G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000362079.2:n.746G>A ENSP00000354982.2:p.Ter249=