Allele Registry

Canonical Allele Identifier: PA2573063454

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000024004

RCV000086836

RCV002468978

ClinVar Variation:

31012

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ser1783Ala	CA228715 NM_000552.5:c.5347T>G