TNNC2:Ensemblv115

troponin C2, fast skeletal type
OMIM: 191039, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber TNNC2 in Muscular dystrophy and myopathy_Paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Expert Review Green
  • Other
  • Expert Review Amber
Phenotypes
  • Congenital Myopathy 15 (MIM#62016)