PC c.2431_2433delinsTGT ;(p.G811C)

Variant ID: 11-66618185-CCC-ACA

NM_001040716.1(PC):c.2431_2433delinsTGT;(p.G811C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


DSG2 mutations contribute to arrhythmogenic right ventricular dysplasia/cardiomyopathy.

American Journal Of Human Genetics
Awad, Mark M MM; Dalal, Darshan D; Cho, Eunpi E; Amat-Alarcon, Nuria N; James, Cynthia C; Tichnell, Crystal C; Tucker, April A; Russell, Stuart D SD; Bluemke, David A DA; Dietz, Harry C HC; Calkins, Hugh H; Judge, Daniel P DP
Publication Date: 2006-07

Variant appearance in text: PC: G811C
PubMed Link: 16773573
Variant Present in the following documents:
  • Main text
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