NM_001267550.2(TTN):c.97419T>C (p.Arg32473=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002176034.5
Allele description [Variation Report for NM_001267550.2(TTN):c.97419T>C (p.Arg32473=)]
NM_001267550.2(TTN):c.97419T>C (p.Arg32473=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024