Canonical Allele Identifier: CA120542

Gene:

Linked Data

• ClinVar Variation Id: 9557
• ClinVar RCV Id: RCV000010167 ; RCV002247284
• dbSNP Id: rs199474674
• MyVariant Identifiers: chrMT:g.5532G>A (hg38)
• PubMed: PMID:15054399

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5532G>A , J01415.2:m.5532G>A	GRCh38