NM_001267550.2(TTN):c.63711C>A (p.Thr21237=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002060331.13
Allele description [Variation Report for NM_001267550.2(TTN):c.63711C>A (p.Thr21237=)]
NM_001267550.2(TTN):c.63711C>A (p.Thr21237=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024