VWF c.1909G>C ;(p.G637R)

Variant ID: 12-6166059-C-G

NM_000552.3(VWF):c.1909G>C;(p.G637R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic abnormalities in biopsy-proven, adult-onset hemolytic uremic syndrome and C3 glomerulopathy.

Journal Of Molecular Medicine (Berlin, Germany)
Haydock, Ludwig L; Garneau, Alexandre P AP; Tremblay, Laurence L; Yen, Hai-Yun HY; Gao, Hanlin H; Harrisson, Raphaƫl R; Isenring, Paul P
Publication Date: 2022-02

Variant appearance in text: VWF: Gly637Arg
PubMed Link: 34714369
Variant Present in the following documents:
  • 109_2021_Article_2102.pdf
View BVdb publication page