NM_001040142.2(SCN2A):c.4665G>C (p.Gln1555His) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003798388.2
Allele description [Variation Report for NM_001040142.2(SCN2A):c.4665G>C (p.Gln1555His)]
NM_001040142.2(SCN2A):c.4665G>C (p.Gln1555His)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024