Canonical Allele Identifier: PA2573063333
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100329
ClinVar RCV Id: RCV000086734 RCV000678770 RCV002222016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1374Cys
CA228539
NM_000552.5:c.4120C>T