Allele Registry

Canonical Allele Identifier: PA2573063299

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086707

ClinVar Variation:

100306

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ser1310Phe	CA228494 NM_000552.5:c.3929C>T