Canonical Allele Identifier: PA2573063079
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 289
ClinVar RCV Id: RCV000000313 RCV000086703 RCV000851770 RCV002225253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1308Cys
CA114125
NM_000552.5:c.3922C>T