KCNQ1 c.44_45delinsAT ;(p.W15Y)

Variant ID: 11-2466372-GG-AT

NM_000218.2(KCNQ1):c.44_45delinsAT;(p.W15Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Brugada syndrome: a fatal disease with complex genetic etiologies - still a long way to go.

Forensic Sciences Research
Wu, Yeda Y; Ai, Mei M; Bardeesi, Adham Sameer A ASA; Xu, Lunwu L; Zheng, Jingjing J; Zheng, Da D; Yin, Kun K; Wu, Qiuping Q; Zhang, Liyong L; Huang, Lei L; Cheng, Jianding J
Publication Date: 2017

Variant appearance in text: KCNQ1: W15Y
PubMed Link: 30483629
Variant Present in the following documents:
  • Main text
  • tfsr-2-1333203.pdf
View BVdb publication page