NM_001267550.2(TTN):c.101766G>C (p.Gln33922His) AND none provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 17, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001283579.2
Allele description
NM_001267550.2(TTN):c.101766G>C (p.Gln33922His)
Condition(s)
- Name:
- none provided
- Identifiers:
- MedGen: CN235283
Assertion and evidence details
Last Updated: Jan 15, 2022