Canonical Allele Identifier: CA658799935

Gene:

Linked Data

• ClinVar Variation Id: 517363
• ClinVar RCV Id: RCV000600524
• dbSNP Id: rs1556422518
• MyVariant Identifiers: chrMT:g.1299A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1299A>G , J01415.2:m.1299A>G	GRCh38