Allele Registry

Canonical Allele Identifier: PA2573063223

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086623

ClinVar Variation:

100231

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Asp879Asn	CA228357 NM_000552.5:c.2635G>A