KCNH2 c.982C>G ;(p.R328G)

Variant ID: 7-150654525-G-C

NM_000238.3(KCNH2):c.982C>G;(p.R328G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes.

Ebiomedicine
Campuzano, Oscar O; Sarquella-Brugada, Georgia G; Fernandez-Falgueras, Anna A; Coll, Mónica M; Iglesias, Anna A; Ferrer-Costa, Carles C; Cesar, Sergi S; Arbelo, Elena E; García-Álvarez, Ana A; Jordà, Paloma P; Toro, Rocío R; Tiron de Llano, Coloma C; Grassi, Simone S; Oliva, Antonio A; Brugada, Josep J; Brugada, Ramon R
Publication Date: 2020-04

Variant appearance in text: KCNH2: 982C>G; Arg328Gly
PubMed Link: 32268277
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page