Canonical Allele Identifier: CA254839

Gene:

Linked Data

• ClinVar Variation Id: 9590
• ClinVar RCV Id: RCV000010212 ; RCV000507161 ; RCV000763624 ; RCV003319163
• dbSNP Id: rs199474658
• MyVariant Identifiers: chrMT:g.3271T>C (hg38)
• PubMed: PMID:1932147 ; PMID:8280119 ; PMID:16006433

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3271T>C , J01415.2:m.3271T>C	GRCh38