NM_001267550.2(TTN):c.96723C>G (p.Ala32241=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 5, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000733506.4
Allele description [Variation Report for NM_001267550.2(TTN):c.96723C>G (p.Ala32241=)]
NM_001267550.2(TTN):c.96723C>G (p.Ala32241=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024