NM_001267550.2(TTN):c.77205G>A (p.Val25735=) AND Cardiovascular phenotype
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 17, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000618047.3
Allele description [Variation Report for NM_001267550.2(TTN):c.77205G>A (p.Val25735=)]
NM_001267550.2(TTN):c.77205G>A (p.Val25735=)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Oct 20, 2024