KCNH2 c.2671T>A ;(p.F891I)

Variant ID: 7-150645553-A-T

NM_000238.3(KCNH2):c.2671T>A;(p.F891I)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Correlations between clinical and physiological consequences of the novel mutation R878C in a highly conserved pore residue in the cardiac Na+ channel.

Acta Physiologica (Oxford, England)
Zhang, Y Y; Wang, T T; Ma, A A; Zhou, X X; Gui, J J; Wan, H H; Shi, R R; Huang, C C; Grace, A A AA; Huang, C L-H CL; Trump, D D; Zhang, H H; Zimmer, T T; Lei, M M
Publication Date: 2008-12

Variant appearance in text: LQT2: F891I
PubMed Link: 18616619
Variant Present in the following documents:
  • Main text
  • aps0194-0311.pdf
View BVdb publication page