NM_001182.5(ALDH7A1):c.1567A>G (p.Thr523Ala) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 13, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002312713.9
Allele description [Variation Report for NM_001182.5(ALDH7A1):c.1567A>G (p.Thr523Ala)]
NM_001182.5(ALDH7A1):c.1567A>G (p.Thr523Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Nov 24, 2024