TNNT2

Name
TNNT2
HGNC ID
HGNC:11949
Cytogenetic Location
1q32.1
Haploinsufficiency
No Evidence
Triplosensitivity
No Evidence
External Resources
View external resources
ClinVar Variants
View ClinVar Variants
GeneReviews®
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Curated by Classification Date Report
Clinicalvalidity on Gene-Disease Validity Definitive
Autosomal Dominant 11/07/2017 View report
Curated by Classification Date Report
Clinicalactionability on Clinical Actionability View report for scoring details 01/09/2018 View report
Curated by Classification Date Report
Clinicalactionability on Clinical Actionability View report for scoring details 01/11/2018 View report