NM_001267550.2(TTN):c.7961G>A (p.Arg2654Lys) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 25, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001703910.1
Allele description [Variation Report for NM_001267550.2(TTN):c.7961G>A (p.Arg2654Lys)]
NM_001267550.2(TTN):c.7961G>A (p.Arg2654Lys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024