GRIN2A c.4135A>G ;(p.I1379V)

Variant ID: 16-9857266-T-C

NM_001134407.1(GRIN2A):c.4135A>G;(p.I1379V)

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:

Mutations of N-Methyl-D-Aspartate Receptor Subunits in Epilepsy.

Neuroscience Bulletin
Xu, Xing-Xing XX; Luo, Jian-Hong JH
Publication Date: 2018-06

Variant appearance in text: GRIN2A: 4135A>G
PubMed Link: 29124671
Variant Present in the following documents:
  • Main text
View BVdb publication page