TNNC2

Panel	Reviews	Mode of inheritance	Details
Green TNNC2 in Mendeliome Version 1.1891	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Myopathy, congenital, with neonatal respiratory insufficiency, MIM# 620161
Amber TNNC2 in Muscular dystrophy and myopathy_Paediatric Level 2: Neurology and neurodevelopmental disorders Version 1.33 Component of the following Super Panels: Myopathy Superpanel Neuromuscular Superpanel	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Other Expert Review Green Literature Phenotypes Congenital Myopathy 15 (MIM#62016)

Panel

Reviews

Mode of inheritance

Details

Version 1.1891

review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

Myopathy Superpanel

Neuromuscular Superpanel

review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

2 panels