NM_001040142.2(SCN2A):c.4871T>C (p.Leu1624Pro) AND multiple conditions
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Oct 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002842714.2
Allele description [Variation Report for NM_001040142.2(SCN2A):c.4871T>C (p.Leu1624Pro)]
NM_001040142.2(SCN2A):c.4871T>C (p.Leu1624Pro)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024