NM_001267550.2(TTN):c.39689C>T (p.Ala13230Val) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 28, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001086600.7
Allele description [Variation Report for NM_001267550.2(TTN):c.39689C>T (p.Ala13230Val)]
NM_001267550.2(TTN):c.39689C>T (p.Ala13230Val)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024