Allele Registry

Canonical Allele Identifier: PA2573171085

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV002244540

ClinVar Variation:

1684018

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ile1628Asn	CA383498769 NM_000552.5:c.4883T>A