NM_001267550.2(TTN):c.7817C>T (p.Ala2606Val) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- May 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000997591.25
Allele description [Variation Report for NM_001267550.2(TTN):c.7817C>T (p.Ala2606Val)]
NM_001267550.2(TTN):c.7817C>T (p.Ala2606Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Nov 24, 2024