Canonical Allele Identifier: CA120568

Gene:

Linked Data

• ClinVar Variation Id: 9598
• ClinVar RCV Id: RCV000010221 ; RCV000850703 ; RCV002288480
• dbSNP Id: rs199474666
• MyVariant Identifiers: chrMT:g.3274A>G (hg38)
• ERepo: CA120568/MONDO:0044970/014
• PubMed: PMID:11723298

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3274A>G , J01415.2:m.3274A>G	GRCh38