Canonical Allele Identifier: CA16040644
Gene:

Linked Data

ClinVar Variation Id: 370043
dbSNP Id: rs1057516055
MyVariant Identifiers: chrMT:g.1661A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1661A>G , J01415.2:m.1661A>G GRCh38