F8 c.5292G>A ;(p.Q1764=)

Variant ID: X-154134776-C-T

NM_000132.3(F8):c.5292G>A;(p.Q1764=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Three novel F8 mutations in sporadic haemophilia A cases.

Springerplus
Hussain, Rashid R; Abid, Noman Bin NB; Hussain, Sajjad S; Shaukat, Zeeshan Z; Altaf, Mudassir M; Altaf, Sara S; Niazi, Gulzar G
Publication Date: 2012

Variant appearance in text: rs5986891
PubMed Link: 23961341
Variant Present in the following documents:
  • Main text
View BVdb publication page