VWF c.2092A>T ;(p.R698W)

Variant ID: 12-6161803-T-A

NM_000552.3(VWF):c.2092A>T;(p.R698W)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutations in intron 1 and intron 22 inversion negative haemophilia A patients from Western India.

Plos One
Nair, Preethi S PS; Shetty, Shrimati D SD; Chandrakala, S S; Ghosh, Kanjaksha K
Publication Date: 2014

Variant appearance in text: VWF: Arg698Trp
PubMed Link: 24845853
Variant Present in the following documents:
  • Main text
  • pone.0097337.pdf
View BVdb publication page