Canonical Allele Identifier: CA915952050

Gene:

Linked Data

• ClinVar Variation Id: 638146
• ClinVar RCV Id: RCV000790614

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8480_13440del , J01415.2:m.8480_13440del	GRCh38