Canonical Allele Identifier: PA2573063374
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 440408
ClinVar RCV Id: RCV000506081 RCV002264704
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1499Glu
CA383501687
NM_000552.5:c.4496T>A