Canonical Allele Identifier: PA2573063277
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100281
ClinVar RCV Id: RCV000086678 RCV002243726 RCV002243727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.His1268Asp
CA228445
NM_000552.5:c.3802C>G