Canonical Allele Identifier: CA254841

Gene:

Linked Data

• ClinVar Variation Id: 9603
• ClinVar RCV Id: RCV000010226 ; RCV000022900 ; RCV000224071 ; RCV000223744 ; RCV000850718
• dbSNP Id: rs121434467
• MyVariant Identifiers: chrMT:g.4295A>G (hg38)
• PubMed: PMID:8889580 ; PMID:22241583

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4295A>G , J01415.2:m.4295A>G	GRCh38