NM_004974.4(KCNA2):c.1392T>G (p.Gly464=) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 12, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002316468.9
Allele description [Variation Report for NM_004974.4(KCNA2):c.1392T>G (p.Gly464=)]
NM_004974.4(KCNA2):c.1392T>G (p.Gly464=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Aug 18, 2024