NM_001267550.2(TTN):c.7817C>T (p.Ala2606Val) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002400169.3
Allele description [Variation Report for NM_001267550.2(TTN):c.7817C>T (p.Ala2606Val)]
NM_001267550.2(TTN):c.7817C>T (p.Ala2606Val)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Nov 24, 2024