NM_015175.3(NBEAL2):c.402G>A (p.Val134=) AND NBEAL2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 22, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003974289.1
Allele description [Variation Report for NM_015175.3(NBEAL2):c.402G>A (p.Val134=)]
NM_015175.3(NBEAL2):c.402G>A (p.Val134=)
Condition(s)
- Name:
- NBEAL2-related disorder
- Synonyms:
- NBEAL2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024