KCNH2 c.1192T>C ;(p.W398R)

Variant ID: 7-150649878-A-G

NM_000238.3(KCNH2):c.1192T>C;(p.W398R)

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:

QT Adaptation and Intrinsic QT Variability in Congenital Long QT Syndrome.

Journal Of The American Heart Association
Seethala, Srikanth S; Singh, Prabhpreet P; Shusterman, Vladimir V; Ribe, Margareth M; Haugaa, Kristina H KH; Němec, Jan J
Publication Date: 2015-12-16

Variant appearance in text: LQT2: 1192T>C
PubMed Link: 26675252
Variant Present in the following documents:
  • Main text
  • JAH3-4-e002395.pdf
View BVdb publication page