Allele Registry

Canonical Allele Identifier: PA2573063366

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086760

RCV002466430

ClinVar Variation:

100355

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Pro1462Ala	CA228590 NM_000552.5:c.4384C>G