NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys) AND Primary familial hypertrophic cardiomyopathy
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Jul 20, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000148898.13
Allele description [Variation Report for NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys)]
NM_001276345.2(TNNT2):c.862C>T (p.Arg288Cys)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024