NM_001276345.2(TNNT2):c.844C>T (p.Gln282Ter) AND Hypertrophic cardiomyopathy 2
- Germline classification:
- Uncertain significance (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:
- RCV003451802.1
Allele description [Variation Report for NM_001276345.2(TNNT2):c.844C>T (p.Gln282Ter)]
NM_001276345.2(TNNT2):c.844C>T (p.Gln282Ter)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024