Allele Registry

Canonical Allele Identifier: PA2573063358

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086751

RCV002227446

RCV002498470

ClinVar Variation:

100346

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ile1425Phe	CA228573 NM_000552.5:c.4273A>T