Canonical Allele Identifier: CA10581201
Gene:

Linked Data

ClinVar Variation Id: 235013
dbSNP Id: rs876661359
MyVariant Identifiers: chrMT:g.4315A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4315A>G , J01415.2:m.4315A>G GRCh38