Canonical Allele Identifier: CA120545

Gene:

Linked Data

• ClinVar Variation Id: 9561
• ClinVar RCV Id: RCV000010173 ; RCV002247285
• dbSNP Id: rs118203889
• MyVariant Identifiers: chrMT:g.12207G>A (hg38)
• PubMed: PMID:16950817

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12207G>A , J01415.2:m.12207G>A	GRCh38