Allele Registry

Canonical Allele Identifier: PA2573063303

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086711

ClinVar Variation:

100309

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Val1314Asp	CA228500 NM_000552.5:c.3941T>A