NM_001267550.2(TTN):c.9472-19dup AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002187299.6
Allele description [Variation Report for NM_001267550.2(TTN):c.9472-19dup]
NM_001267550.2(TTN):c.9472-19dup
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024