Canonical Allele Identifier: CA10581195

Gene:

Linked Data

• ClinVar Variation Id: 235016
• ClinVar RCV Id: RCV000223921
• dbSNP Id: rs876661362
• MyVariant Identifiers: chrMT:g.3276A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3276A>G , J01415.2:m.3276A>G	GRCh38