KCNH2 c.526_527delinsAC ;(p.R176T)

Variant ID: 7-150655536-CG-GT

NM_000238.3(KCNH2):c.526_527delinsAC;(p.R176T)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Variable Clinical Appearance of the Kir2.1 Rare Variants in Russian Patients with Long QT Syndrome.

Genes
Zaklyazminskaya, Elena E; Polyak, Margarita M; Shestak, Anna A; Sadekova, Mariam M; Komoliatova, Vera V; Kiseleva, Irina I; Makarov, Leonid L; Podolyak, Dmitriy D; Glukhov, Grigory G; Zhang, Han H; Abramochkin, Denis D; Sokolova, Olga S OS
Publication Date: 2022-03-22

Variant appearance in text: KCNH2: R176T
PubMed Link: 35456365
Variant Present in the following documents:
  • Main text
  • genes-13-00559.pdf
View BVdb publication page