Canonical Allele Identifier: CA337095924
Gene:

Linked Data

dbSNP Id: rs879005843
MyVariant Identifiers: chrMT:g.669T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.669T>C , J01415.2:m.669T>C GRCh38