Canonical Allele Identifier: CA254833
Gene:

Linked Data

ClinVar Variation Id: 9571
dbSNP Id: rs199474700
MyVariant Identifiers: chrMT:g.15965A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15965A>G , J01415.2:m.15965A>G GRCh38