Canonical Allele Identifier: PA2573063398
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100381
ClinVar RCV Id: RCV000086787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Leu1562Pro
CA228637
NM_000552.5:c.4685T>C