Canonical Allele Identifier: PA2573063281
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 301
ClinVar RCV Id: RCV000000328 RCV000086679 RCV002243607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys1272Arg
CA114149
NM_000552.5:c.3814T>C