Canonical Allele Identifier: CA337096477

Gene:

Linked Data

• ClinVar Variation Id: 689868
• ClinVar RCV Id: RCV000850707
• dbSNP Id: rs386828902
• MyVariant Identifiers: chrMT:g.3277G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3277G>A , J01415.2:m.3277G>A	GRCh38