NM_001365536.1(SCN9A):c.1347T>C (p.Ser449=) AND Paroxysmal extreme pain disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000269918.5
Allele description [Variation Report for NM_001365536.1(SCN9A):c.1347T>C (p.Ser449=)]
NM_001365536.1(SCN9A):c.1347T>C (p.Ser449=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024