NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) AND Paroxysmal extreme pain disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000276938.6
Allele description [Variation Report for NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val)]
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val)
Condition(s)
Assertion and evidence details
Last Updated: May 12, 2024