Canonical Allele Identifier: PA2573063380
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100369
ClinVar RCV Id: RCV000086774 RCV000852128 RCV002222018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ser1506Leu
CA228615
NM_000552.5:c.4517C>T