Allele Registry

Canonical Allele Identifier: PA3057451595

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV004997945

ClinVar Variation:

3572153

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.His484Leu	CA6403396 NM_000552.5:c.1451A>T