NM_001134407.3(GRIN2A):c.3091G>T (p.Val1031Phe) AND GRIN2A-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003982663.1
Allele description [Variation Report for NM_001134407.3(GRIN2A):c.3091G>T (p.Val1031Phe)]
NM_001134407.3(GRIN2A):c.3091G>T (p.Val1031Phe)
Condition(s)
- Name:
- GRIN2A-related disorder
- Synonyms:
- GRIN2A-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024