Allele Registry

Canonical Allele Identifier: PA2573063413

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000000309

RCV000086797

RCV000623564

RCV000851942

RCV000999877

RCV002243603

ClinVar Variation:

285

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg1597Trp	CA114117 NM_000552.5:c.4789C>T