Allele Registry

Canonical Allele Identifier: PA2573063339

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086738

RCV000778378

RCV002243738

RCV002264660

RCV003335097

ClinVar Variation:

100333

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg1379Cys	CA228547 NM_000552.5:c.4135C>T