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TNNC2

troponin C2, fast skeletal type

HCNC Approved Symbol
TNNC2 (HGNC:11944)
Genomic Coordinates
20:45,823,214 - 45,833,306 (20q13.12)
Synonyms
FAP85, CFAP85
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Congenital myopathy 15
620161AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the TNNC2 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results