Canonical Allele Identifier: CA337100598
Gene:

Linked Data

ClinVar Variation Id: 690250
ClinVar RCV Id: RCV000851144
dbSNP Id: rs879197567
MyVariant Identifiers: chrMT:g.15940T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15940T>C , J01415.2:m.15940T>C GRCh38