Canonical Allele Identifier: PA2573063335
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100331
ClinVar RCV Id: RCV000086736 RCV002243737 RCV002264659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1374Leu
CA228543
NM_000552.5:c.4121G>T