Canonical Allele Identifier: PA2573063241
Gene: VWF HGNC NCBI

Linked Data

ClinVar Variation Id: 100250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000543.3:p.Glu1078Lys
CA228384
NM_000552.5:c.3232G>A