Canonical Allele Identifier: CA280144

Gene:

Linked Data

• ClinVar Variation Id: 9600
• ClinVar RCV Id: RCV000010223 ; RCV000850687
• dbSNP Id: rs193303018
• MyVariant Identifiers: chrMT:g.3242G>A (hg38)
• PubMed: PMID:14576046 ; PMID:20550934

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3242G>A , J01415.2:m.3242G>A	GRCh38