Canonical Allele Identifier: CA645373344

Gene:

Linked Data

• ClinVar Variation Id: 430688
• ClinVar RCV Id: RCV000495226
• dbSNP Id: rs1131692062
• MyVariant Identifiers: chrMT:g.12283G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12283G>A , J01415.2:m.12283G>A	GRCh38