Canonical Allele Identifier: CA913180561

Gene:

Linked Data

• ClinVar Variation Id: 690006
• ClinVar RCV Id: RCV000850864
• dbSNP Id: rs1556423041

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5822G>A , J01415.2:m.5822G>A	GRCh38