Canonical Allele Identifier: CA337096439

Gene:

Linked Data

• dbSNP Id: rs28408321
• MyVariant Identifiers: chrMT:g.3126C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3126C>G , J01415.2:m.3126C>G	GRCh38