Canonical Allele Identifier: CA254837
Gene:

Linked Data

ClinVar Variation Id: 9583
dbSNP Id: rs118192101
MyVariant Identifiers: chrMT:g.8313G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8313G>A , J01415.2:m.8313G>A GRCh38