Canonical Allele Identifier: PA2573063321
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100316
ClinVar RCV Id: RCV000086720 RCV002243735 RCV002280870 RCV003323398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1341Trp
CA228514
NM_000552.5:c.4021C>T