Canonical Allele Identifier: CA337100665
Gene:

Linked Data

dbSNP Id: rs41534744
MyVariant Identifiers: chrMT:g.16129G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16129G>C , J01415.2:m.16129G>C GRCh38