NM_001267550.2(TTN):c.89989T>A (p.Leu29997Met) AND Cardiovascular phenotype
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Mar 31, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002354376.2
Allele description [Variation Report for NM_001267550.2(TTN):c.89989T>A (p.Leu29997Met)]
NM_001267550.2(TTN):c.89989T>A (p.Leu29997Met)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Oct 20, 2024