NM_001276345.2(TNNT2):c.427G>C (p.Glu143Gln) AND Cardiomyopathy, familial restrictive, 3
- 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:
- RCV003449620.1
Allele description [Variation Report for NM_001276345.2(TNNT2):c.427G>C (p.Glu143Gln)]
NM_001276345.2(TNNT2):c.427G>C (p.Glu143Gln)
Condition(s)
Assertion and evidence details
Last Updated: Sep 16, 2024