TNNT2 c.154A>G ;(p.R52G)

Variant ID: 1-201337299-T-C

NM_001276345.1(TNNT2):c.154A>G;(p.R52G)

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:

Potential Common Pathogenic Pathways for the Left Ventricular Noncompaction Cardiomyopathy (LVNC).

Pediatric Cardiology
Liu, Ying Y; Chen, Hanying H; Shou, Weinian W
Publication Date: 2018-08

Variant appearance in text: TNNT2: R52G
PubMed Link: 29766225
Variant Present in the following documents:
  • Main text
View BVdb publication page