Canonical Allele Identifier: PA2573063219
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100228
ClinVar RCV Id: RCV000086619 RCV001787049 RCV004017399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg854Trp
CA228351
NM_000552.5:c.2560C>T