NM_130837.3(OPA1):c.1302T>G (p.Pro434=) AND Autosomal dominant optic atrophy classic form
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000277400.6
Allele description [Variation Report for NM_130837.3(OPA1):c.1302T>G (p.Pro434=)]
NM_130837.3(OPA1):c.1302T>G (p.Pro434=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024