NM_001267550.2(TTN):c.76722T>C (p.Tyr25574=) AND Early-onset myopathy with fatal cardiomyopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000269503.13
Allele description [Variation Report for NM_001267550.2(TTN):c.76722T>C (p.Tyr25574=)]
NM_001267550.2(TTN):c.76722T>C (p.Tyr25574=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024