Allele Registry

Canonical Allele Identifier: PA2573063559

Gene: VWF HGNC NCBI

ClinVar Variation Id: 501149

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Asn2679Ser	CA6401416 NM_000552.5:c.8036A>G