Canonical Allele Identifier: PA2573063075
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100300
ClinVar RCV Id: RCV000086700 RCV002243729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1306Gln
CA228482
NM_000552.5:c.3917G>A