Canonical Allele Identifier: CA337100776
Gene:

Linked Data

dbSNP Id: rs386829281
MyVariant Identifiers: chrMT:g.16220A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16220A>C , J01415.2:m.16220A>C GRCh38