Canonical Allele Identifier: PA2573063290
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 311
ClinVar RCV Id: RCV000000339 RCV000086691
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ser1285Phe
CA114164
NM_000552.5:c.3854C>T