Canonical Allele Identifier: PA2573063291
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100294
ClinVar RCV Id: RCV000086693 RCV000851986 RCV002264652 RCV002264651
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Leu1288Arg
CA228470
NM_000552.5:c.3863T>G