Allele Registry

Canonical Allele Identifier: PA2573063320

Gene: VWF HGNC NCBI

ClinVar Allele:

106194

ClinVar RCV:

RCV000086722

RCV002264656

ClinVar Variation:

100317

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg1341Pro	CA228516 NM_000552.5:c.4022G>C