GRIN2A c.56G>A ;(p.R19H)

Variant ID: 16-10274213-C-T

NM_001134407.1(GRIN2A):c.56G>A;(p.R19H)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

A Systems Biology Approach for Personalized Medicine in Refractory Epilepsy.

International Journal Of Molecular Sciences
Naimo, Giuseppina Daniela GD; Guarnaccia, Maria M; Sprovieri, Teresa T; Ungaro, Carmine C; Conforti, Francesca Luisa FL; Andò, Sebastiano S; Cavallaro, Sebastiano S
Publication Date: 2019-07-30

Variant appearance in text:
PubMed Link: 31366017
Variant Present in the following documents:
  • ijms-20-03717-s001.pdf
View BVdb publication page