KCNH2 c.91A>T ;(p.I31F)

Variant ID: 7-150672015-T-A

NM_000238.3(KCNH2):c.91A>T;(p.I31F)

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:

Assessment of microvolt T-wave alternans in high-risk patients with the congenital long-QT syndrome.

Annals Of Noninvasive Electrocardiology : The Official Journal Of The International Society For Holter And Noninvasive Electrocardiology, Inc
Schmitt, Jörn J; Baumann, Stefan S; Klingenheben, Thomas T; Richter, Sergio S; Duray, Gabor G; Hohnloser, Stefan H SH; Ehrlich, Joachim R JR
Publication Date: 2009-10

Variant appearance in text: KCNH2: 91A>T; Ile31Phe
PubMed Link: 19804510
Variant Present in the following documents:
  • Main text
View BVdb publication page