Canonical Allele Identifier: CA337100868

Gene:

Linked Data

• dbSNP Id: rs144417390
• MyVariant Identifiers: chrMT:g.16292C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.16292C>T , J01415.2:m.16292C>T	GRCh38