Canonical Allele Identifier: PA2573063082
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100310
ClinVar RCV Id: RCV000086712 RCV000851600 RCV002243732 RCV002264655 RCV004549529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1315Cys
CA228502
NM_000552.5:c.3943C>T