Canonical Allele Identifier: PA2499233422
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 1098555
ClinVar RCV Id: RCV001420489
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ile1677Val
CA383498466
NM_000552.5:c.5029A>G