NM_001267550.2(TTN):c.55986C>T (p.Val18662=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000593469.8
Allele description [Variation Report for NM_001267550.2(TTN):c.55986C>T (p.Val18662=)]
NM_001267550.2(TTN):c.55986C>T (p.Val18662=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 5, 2023