NM_001265589.2(RTN3):c.177A>C (p.Val59=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 1, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000891650.3
Allele description [Variation Report for NM_001265589.2(RTN3):c.177A>C (p.Val59=)]
NM_001265589.2(RTN3):c.177A>C (p.Val59=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023