Canonical Allele Identifier: PA2573063585
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100507
ClinVar RCV Id: RCV000086922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2804Tyr
CA228855
NM_000552.5:c.8411G>A