Canonical Allele Identifier: PA2573063286
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100288
ClinVar RCV Id: RCV000086686 RCV000851984 RCV002222388 RCV003987361 RCV003313778 RCV002280868
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Val1279Ile
CA228459
NM_000552.5:c.3835G>A