Canonical Allele Identifier: PA2573063073
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 308
ClinVar RCV Id: RCV000000335 RCV000000336 RCV000086666 RCV000851598 RCV001003906 RCV004547447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1205His
CA114160
NM_000552.5:c.3614G>A