Canonical Allele Identifier: CA658799930

Gene:

Linked Data

• ClinVar Variation Id: 517649
• ClinVar RCV Id: RCV000600321
• dbSNP Id: rs1556422506
• MyVariant Identifiers: chrMT:g.1047A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1047A>G , J01415.2:m.1047A>G	GRCh38