Canonical Allele Identifier: PA2573063561
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100489
ClinVar RCV Id: RCV000086903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2693Tyr
CA228823
NM_000552.5:c.8078G>A