NM_001083619.3(GRIA2):c.523G>C (p.Val175Leu) AND GRIA2-related condition
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 29, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003422455.4
Allele description [Variation Report for NM_001083619.3(GRIA2):c.523G>C (p.Val175Leu)]
NM_001083619.3(GRIA2):c.523G>C (p.Val175Leu)
Condition(s)
- Name:
- GRIA2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Mar 10, 2024