Canonical Allele Identifier: PA2741815791
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 3061402
ClinVar RCV Id: RCV004548986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Leu1340Pro
CA383505745
NM_000552.5:c.4019T>C