Canonical Allele Identifier: PA2573063411
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100391
ClinVar RCV Id: RCV000086799 RCV000852141 RCV002243742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1597Gln
CA228657
NM_000552.5:c.4790G>A