Canonical Allele Identifier: CA120556

Gene:

Linked Data

• ClinVar Variation Id: 9582
• ClinVar RCV Id: RCV000010198 ; RCV000223829
• dbSNP Id: rs118192103
• MyVariant Identifiers: chrMT:g.8342G>A (hg38)
• PubMed: PMID:10220860

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8342G>A , J01415.2:m.8342G>A	GRCh38