Canonical Allele Identifier: CA337096024

Gene:

Linked Data

• dbSNP Id: rs28496470
• MyVariant Identifiers: chrMT:g.1273G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1273G>T , J01415.2:m.1273G>T	GRCh38