NM_001267550.2(TTN):c.54874G>C (p.Gly18292Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 24, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000172310.1
Allele description [Variation Report for NM_001267550.2(TTN):c.54874G>C (p.Gly18292Arg)]
NM_001267550.2(TTN):c.54874G>C (p.Gly18292Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 4, 2024