Canonical Allele Identifier: PA2573063330
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100326
ClinVar RCV Id: RCV000086731 RCV000851784 RCV002222390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Phe1369Ile
CA228533
NM_000552.5:c.4105T>A