Allele Registry

Canonical Allele Identifier: PA2573063078

Gene: VWF HGNC NCBI

ClinVar Variation Id: 100301

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg1306Leu	CA228484 NM_000552.5:c.3917G>T