Canonical Allele Identifier: PA2573063227
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100240
ClinVar RCV Id: RCV000086632 RCV001787051 RCV002243720 RCV002243719 RCV003447494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg924Gln
CA228368
NM_000552.5:c.2771G>A