Canonical Allele Identifier: PA2573063215
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 295
ClinVar RCV Id: RCV000000319 RCV000086613 RCV001195286
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg816Trp
CA114137
NM_000552.5:c.2446C>T