Canonical Allele Identifier: CA120565

Gene:

Linked Data

• ClinVar Variation Id: 9595
• ClinVar RCV Id: RCV000010218 ; RCV000850691
• dbSNP Id: rs199474662
• MyVariant Identifiers: chrMT:g.3251A>G (hg38)
• PubMed: PMID:8265770 ; PMID:8786060

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3251A>G , J01415.2:m.3251A>G	GRCh38