Canonical Allele Identifier: PA2573063151
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 291166
ClinVar RCV Id: RCV000319239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val444Ile
CA6403449
NM_000552.5:c.1330G>A