NM_001267550.2(TTN):c.91643C>T (p.Ala30548Val) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Aug 1, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000184979.5
Allele description
NM_001267550.2(TTN):c.91643C>T (p.Ala30548Val)
Condition(s)
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Dec 12, 2021