Canonical Allele Identifier: CA120559

Gene:

Linked Data

• ClinVar Variation Id: 9588
• ClinVar RCV Id: RCV000010205 ; RCV000851078 ; RCV000844938
• dbSNP Id: rs121434464
• MyVariant Identifiers: chrMT:g.12297T>C (hg38)
• PubMed: PMID:10602359 ; PMID:11313776

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12297T>C , J01415.2:m.12297T>C	GRCh38