Canonical Allele Identifier: PA2573063278
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100284
ClinVar RCV Id: RCV000086682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys1272Ser
CA228451
NM_000552.5:c.3815G>C
CA383507005
NM_000552.5:c.3814T>A