Canonical Allele Identifier: PA2573063390
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100376
ClinVar RCV Id: RCV000086782 RCV002222391
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ser1543Phe
CA228628
NM_000552.5:c.4628C>T