Canonical Allele Identifier: CA356575
Gene:

Identifiers and link-outs to other resources

ClinVar Variation Id: 65516
ClinVar RCV Id: RCV000055705
dbSNP Id: rs869025187
MyVariant Identifiers: chrMT:g.14279G>A (hg38)

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14279G>A , J01415.2:m.14279G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361681.2:n.395C>T ENSP00000354665.2:p.Ser132Leu