NM_001110556.2(FLNA):c.7903G>A (p.Glu2635Lys) AND Abnormality of neuronal migration
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 31, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000201336.2
Allele description [Variation Report for NM_001110556.2(FLNA):c.7903G>A (p.Glu2635Lys)]
NM_001110556.2(FLNA):c.7903G>A (p.Glu2635Lys)
Condition(s)
- Name:
- Abnormality of neuronal migration
- Identifiers:
- MedGen: C1837249; Human Phenotype Ontology: HP:0002269
Assertion and evidence details
Last Updated: Apr 15, 2024