Allele Registry

Canonical Allele Identifier: PA2573063447

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000086831

RCV002271338

ClinVar Variation:

100421

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Trp1745Cys	CA228706 NM_000552.5:c.5235G>T CA383496187 NM_000552.5:c.5235G>C