Canonical Allele Identifier: PA2573063339
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100333
ClinVar RCV Id: RCV000086738 RCV000778378 RCV002264660 RCV002243738 RCV003335097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Arg1379Cys
CA228547
NM_000552.5:c.4135C>T