KCNH2 c.2563A>C ;(p.S855R)

Variant ID: 7-150645973-T-G

NM_000238.3(KCNH2):c.2563A>C;(p.S855R)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic analysis, in silico prediction, and family segregation in long QT syndrome.

European Journal Of Human Genetics : Ejhg
Riuró, Helena H; Campuzano, Oscar O; Berne, Paola P; Arbelo, Elena E; Iglesias, Anna A; Pérez-Serra, Alexandra A; Coll-Vidal, Mònica M; Partemi, Sara S; Mademont-Soler, Irene I; Picó, Ferran F; Allegue, Catarina C; Oliva, Antonio A; Gerstenfeld, Edward E; Sarquella-Brugada, Georgia G; Castro-Urda, Víctor V; Fernández-Lozano, Ignacio I; Mont, Lluís L; Brugada, Josep J; Scornik, Fabiana S FS; Brugada, Ramon R
Publication Date: 2015-01

Variant appearance in text: KCNH2: Ser855Arg
PubMed Link: 24667783
Variant Present in the following documents:
  • Main text
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