KCNH2 c.2686_2687delinsCG ;(p.D896R)

Variant ID: 7-150645537-TC-CG

NM_000238.3(KCNH2):c.2686_2687delinsCG;(p.D896R)

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:

A Novel Frameshift Mutation, KCNH2 [p.Asp896ArgfsX79], Leading to Malignant Ventricular Arrhythmia, Identified After Treatment of Gastrointestinal Bleeding.

Cjc Open
Kim, Wan Cheol WC; Lemire, Edmond E; Nosib, Siddarth S; Nosib, Shravankumar S
Publication Date: 2021-11

Variant appearance in text: KCNH2: Asp896Arg
PubMed Link: 34901807
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page