Canonical Allele Identifier: CA254848
Gene:

Linked Data

ClinVar Variation Id: 9634
dbSNP Id: rs28358569
MyVariant Identifiers: chrMT:g.827A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.827A>G , J01415.2:m.827A>G GRCh38