VWF c.7669T>A ;(p.C2557S)

Variant ID: 12-6078437-A-T

NM_000552.3(VWF):c.7669T>A;(p.C2557S)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


The role of exon 45 and 16 in the pathogenesis of Von Willebrand disease in Iranian Patients.

Iranian Journal Of Pediatric Hematology And Oncology
Nasiri, M M; Galehdari, H H; Darbouy, M M; Yavarian, M M; Keikhaee, B B
Publication Date: 2012

Variant appearance in text: VWF: C2557S
PubMed Link: 24575258
Variant Present in the following documents:
  • Main text
  • ijpho-2-164.pdf
View BVdb publication page