Canonical Allele Identifier: CA913161310

Gene:

Linked Data

• ClinVar Variation Id: 929973
• ClinVar RCV Id: RCV001195339
• dbSNP Id: rs2068677687

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1117A>G , J01415.2:m.1117A>G	GRCh38