KCNQ1 c.940_941delinsTT ;(p.G314F)

Variant ID: 11-2604683-GG-TT

NM_000218.2(KCNQ1):c.940_941delinsTT;(p.G314F)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genotype and clinical characteristics of congenital long QT syndrome in Thailand.

Indian Pacing And Electrophysiology Journal
Saprungruang, Ankavipar A; Khongphatthanayothin, Apichai A; Mauleekoonphairoj, John J; Wandee, Pharawee P; Kanjanauthai, Supaluck S; Bhuiyan, Zahurul A ZA; Wilde, Arthur A M AAM; Poovorawan, Yong Y
Publication Date: 2018

Variant appearance in text: KCNQ1: Gly314Phe
PubMed Link: 30036649
Variant Present in the following documents:
  • Main text
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