Allele Registry

Canonical Allele Identifier: PA2573063220

Gene: VWF HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000000320

RCV000000321

RCV000086620

RCV000169683

RCV000336497

RCV000762901

RCV000851593

RCV001270529

RCV003987302

RCV004547445

ClinVar Variation:

296

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000543.3:p.Arg854Gln	CA114139 NM_000552.5:c.2561G>A