NM_001267550.2(TTN):c.102698A>G (p.Tyr34233Cys) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001056410.8
Allele description [Variation Report for NM_001267550.2(TTN):c.102698A>G (p.Tyr34233Cys)]
NM_001267550.2(TTN):c.102698A>G (p.Tyr34233Cys)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024