Canonical Allele Identifier: CA337100106
Gene:

Linked Data

ClinVar Variation Id: 693744
ClinVar RCV Id: RCV000855131
dbSNP Id: rs41354845
MyVariant Identifiers: chrMT:g.14582A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14582A>G , J01415.2:m.14582A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361681.2:n.92T>C ENSP00000354665.2:p.Val31Ala