Canonical Allele Identifier: CA337096457

Gene:

Linked Data

• dbSNP Id: rs200999343
• MyVariant Identifiers: chrMT:g.3206C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3206C>T , J01415.2:m.3206C>T	GRCh38