Canonical Allele Identifier: CA658799937
Gene:

Linked Data

ClinVar Variation Id: 504960
ClinVar RCV Id: RCV000610384
dbSNP Id: rs1556422534
MyVariant Identifiers: chrMT:g.1461A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1461A>G , J01415.2:m.1461A>G GRCh38