Canonical Allele Identifier: CA120564

Gene:

Linked Data

• ClinVar Variation Id: 9594
• ClinVar RCV Id: RCV000010217 ; RCV000850692
• dbSNP Id: rs199474661
• MyVariant Identifiers: chrMT:g.3252A>G (hg38)
• PubMed: PMID:8111377

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3252A>G , J01415.2:m.3252A>G	GRCh38