Canonical Allele Identifier: PA2573063413
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1597Trp
CA114117
NM_000552.5:c.4789C>T