NF1 c.2390C>G ;(p.A797G)

Variant ID: 17-29554605-C-G

NM_001042492.2(NF1):c.2390C>G;(p.A797G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic Diagnosis in Children with Epilepsy and Developmental Disorders by Targeted Gene Panel Analysis in a Developing Country.

Journal Of Epilepsy Research
Rahman, Md Mizanur MM; Fatema, Kanij K
Publication Date: 2021-06

Variant appearance in text: NF1: 2390C>G
PubMed Link: 34395220
Variant Present in the following documents:
  • Main text
  • jer-21004.pdf
View BVdb publication page