Canonical Allele Identifier: PA2573063346
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100337
ClinVar RCV Id: RCV000086742 RCV000852119 RCV002222017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1399Cys
CA228555
NM_000552.5:c.4195C>T