Canonical Allele Identifier: PA2573063130
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100497
ClinVar RCV Id: RCV000086911 RCV002243755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys275Arg
CA228836
NM_000552.5:c.823T>C