Canonical Allele Identifier: PA2573063340
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 310063
ClinVar RCV Id: RCV000400807 RCV000755447 RCV002244789 RCV002244791 RCV002244790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Ile1380Val
CA6402595
NM_000552.5:c.4138A>G