NM_001267550.2(TTN):c.18054A>C (p.Pro6018=) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000868774.9
Allele description [Variation Report for NM_001267550.2(TTN):c.18054A>C (p.Pro6018=)]
NM_001267550.2(TTN):c.18054A>C (p.Pro6018=)
Condition(s)
Assertion and evidence details
Last Updated: Nov 24, 2024