Allele Registry

Canonical Allele Identifier: PA2573063493

Gene: VWF HGNC NCBI

ClinVar Allele:

106319

ClinVar RCV:

RCV000086854

RCV002264668

ClinVar Variation:

100442

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ser2179Phe	CA228746 NM_000552.5:c.6536C>T