Canonical Allele Identifier: CA254834
Gene:

Linked Data

ClinVar Variation Id: 9573
dbSNP Id: rs118203885
MyVariant Identifiers: chrMT:g.583G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.583G>A , J01415.2:m.583G>A GRCh38