Allele Registry

Canonical Allele Identifier: PA2573063084

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086714

RCV002243733

ClinVar Variation:

100312

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg1315Leu	CA228506 NM_000552.5:c.3944G>T