NM_001165963.4(SCN1A):c.4731T>C (p.Asn1577=) AND Migraine, familial hemiplegic, 3
- Germline classification:
- Likely 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:
- RCV000301218.13
Allele description [Variation Report for NM_001165963.4(SCN1A):c.4731T>C (p.Asn1577=)]
NM_001165963.4(SCN1A):c.4731T>C (p.Asn1577=)
Condition(s)
Assertion and evidence details
Last Updated: Jun 9, 2024