NM_001267550.2(TTN):c.85420C>T (p.Arg28474Cys) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 8, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000474761.4
Allele description [Variation Report for NM_001267550.2(TTN):c.85420C>T (p.Arg28474Cys)]
NM_001267550.2(TTN):c.85420C>T (p.Arg28474Cys)
Condition(s)
Assertion and evidence details
Last Updated: Nov 24, 2024