Canonical Allele Identifier: CA345760
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 143926
ClinVar RCV Id: RCV000133457
MyVariant Identifiers: chrMT:g.15607A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15607A>G , J01415.2:m.15607A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:n.861A>G ENSP00000354554.2:p.Lys287=