Allele Registry

Canonical Allele Identifier: PA2573063093

Gene: VWF HGNC NCBI

ClinVar RCV:

RCV000760135

ClinVar Variation:

619942

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Ala2178Ser	CA6401974 NM_000552.5:c.6532G>T