NM_001267550.2(TTN):c.96934C>T (p.Pro32312Ser) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Oct 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002261701.7
Allele description [Variation Report for NM_001267550.2(TTN):c.96934C>T (p.Pro32312Ser)]
NM_001267550.2(TTN):c.96934C>T (p.Pro32312Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024