NM_001354768.3(NRL):c.585C>G (p.Ala195=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002582869.2
Allele description [Variation Report for NM_001354768.3(NRL):c.585C>G (p.Ala195=)]
NM_001354768.3(NRL):c.585C>G (p.Ala195=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024