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