Canonical Allele Identifier: PA2573063347
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 293
ClinVar RCV Id: RCV000000317 RCV000756907 RCV000851940 RCV001270629 RCV002243606 RCV003234883 RCV003447466 RCV004547444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1399His
CA114133
NM_000552.5:c.4196G>A