Canonical Allele Identifier: PA2573063577
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100503
ClinVar RCV Id: RCV000086918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Cys2773Ser
CA228847
NM_000552.5:c.8318G>C
CA383486646
NM_000552.5:c.8317T>A