Canonical Allele Identifier: CA337100661
Gene:

Linked Data

dbSNP Id: rs147029798
MyVariant Identifiers: chrMT:g.16126T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16126T>C , J01415.2:m.16126T>C GRCh38