TNNC2

Panel	Reviews	Mode of inheritance	Details
Green TNNC2 in Mendeliome Version 1.3512	1 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 1.108 Component of the following Super Panels: Myopathy Superpanel Neuromuscular Superpanel	2 reviews	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 1.3512

1 review

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Level 2: Neurology and neurodevelopmental disorders
Version 1.108

Component of the following Super Panels:

Myopathy Superpanel

Neuromuscular Superpanel

2 reviews

MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

2 panels