KCNH2 c.1756C>A ;(p.L586M)

Variant ID: 7-150648725-G-T

NM_000238.3(KCNH2):c.1756C>A;(p.L586M)

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:

Structures Illuminate Cardiac Ion Channel Functions in Health and in Long QT Syndrome.

Frontiers In Pharmacology
Brewer, Kathryn R KR; Kuenze, Georg G; Vanoye, Carlos G CG; George, Alfred L AL; Meiler, Jens J; Sanders, Charles R CR
Publication Date: 2020

Variant appearance in text: LQT2: L586M
PubMed Link: 32431610
Variant Present in the following documents:
  • Main text
View BVdb publication page