Canonical Allele Identifier: PA2573063248
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100256
ClinVar RCV Id: RCV000086649 RCV000851636 RCV002281057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Trp1120Ser
CA228396
NM_000552.5:c.3359G>C