Canonical Allele Identifier: CA120567

Gene:

Linked Data

• ClinVar Variation Id: 9597
• ClinVar RCV Id: RCV000010220 ; RCV000850710
• dbSNP Id: rs199474665
• MyVariant Identifiers: chrMT:g.3290T>C (hg38)
• PubMed: PMID:10519336

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3290T>C , J01415.2:m.3290T>C	GRCh38