Allele Registry

Canonical Allele Identifier: PA2573063554

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086901

RCV000765101

RCV000851886

RCV002225290

RCV002225291

ClinVar Variation:

100487

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Thr2647Met	CA228819 NM_000552.5:c.7940C>T