Canonical Allele Identifier: PA2573063567
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100495
ClinVar RCV Id: RCV000086909 RCV001787083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2739Tyr
CA228832
NM_000552.5:c.8216G>A