GRIN2D c.1656C>G ;(p.F552L)

Variant ID: 19-48919333-C-G

NM_000836.2(GRIN2D):c.1656C>G;(p.F552L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy.

Neuroscience Bulletin
Wei, Feng F; Yan, Li-Min LM; Su, Tao T; He, Na N; Lin, Zhi-Jian ZJ; Wang, Jie J; Shi, Yi-Wu YW; Yi, Yong-Hong YH; Liao, Wei-Ping WP
Publication Date: 2017-08

Variant appearance in text: GRIN2D: 1656C>G
PubMed Link: 28488083
Variant Present in the following documents:
  • Main text
View BVdb publication page