Allele Registry

Canonical Allele Identifier: PA2573063411

Gene: VWF HGNC NCBI

ClinVar Allele:

106268

ClinVar RCV:

RCV000086799

RCV000852141

RCV002243742

ClinVar Variation:

100391

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg1597Gln	CA228657 NM_000552.5:c.4790G>A