NM_001276345.2(TNNT2):c.861C>A (p.Thr287=) AND Hypertrophic cardiomyopathy 2
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003451542.1
Allele description [Variation Report for NM_001276345.2(TNNT2):c.861C>A (p.Thr287=)]
NM_001276345.2(TNNT2):c.861C>A (p.Thr287=)
Condition(s)
Assertion and evidence details
Last Updated: May 7, 2024