KCNH2 c.1759_1761delinsAAG ;(p.H587K)

Variant ID: 7-150648720-GTG-CTT

NM_000238.3(KCNH2):c.1759_1761delinsAAG;(p.H587K)

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:

Effect of S5P alpha-helix charge mutants on inactivation of hERG K+ channels.

The Journal Of Physiology
Clarke, C E CE; Hill, A P AP; Zhao, J J; Kondo, M M; Subbiah, R N RN; Campbell, T J TJ; Vandenberg, J I JI
Publication Date: 2006-06-01

Variant appearance in text: HERG: H587K
PubMed Link: 16556651
Variant Present in the following documents:
  • Main text
View BVdb publication page