Canonical Allele Identifier: CA645509243

Gene:

Linked Data

• ClinVar Variation Id: 374215
• ClinVar RCV Id: RCV000509005
• dbSNP Id: rs1556423295
• MyVariant Identifiers: chrMT:g.7486G>A (hg38)
• PubMed: PMID:29398297

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.7486G>A , J01415.2:m.7486G>A	GRCh38