NM_001276345.2(TNNT2):c.294+7G>A AND Primary familial hypertrophic cardiomyopathy
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 22, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000030566.9
Allele description [Variation Report for NM_001276345.2(TNNT2):c.294+7G>A]
NM_001276345.2(TNNT2):c.294+7G>A
Condition(s)
Assertion and evidence details
Last Updated: Oct 26, 2024