NM_001267550.2(TTN):c.102193T>C (p.Ser34065Pro) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 23, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001219490.8
Allele description [Variation Report for NM_001267550.2(TTN):c.102193T>C (p.Ser34065Pro)]
NM_001267550.2(TTN):c.102193T>C (p.Ser34065Pro)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024