Canonical Allele Identifier: CA337100125
Gene:

Linked Data

ClinVar Variation Id: 690201
ClinVar RCV Id: RCV000851091
dbSNP Id: rs200189658
MyVariant Identifiers: chrMT:g.14687A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14687A>G , J01415.2:m.14687A>G GRCh38