Canonical Allele Identifier: CA913175448

Gene:

Linked Data

• ClinVar Variation Id: 690273
• ClinVar RCV Id: RCV000851171
• dbSNP Id: rs1603225635

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.16011A>G , J01415.2:m.16011A>G	GRCh38