Canonical Allele Identifier: CA913180702

Gene:

Linked Data

• ClinVar Variation Id: 690019
• ClinVar RCV Id: RCV000850878
• dbSNP Id: rs1603220158

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5864G>A , J01415.2:m.5864G>A	GRCh38