NM_004974.4(KCNA2):c.1392T>G (p.Gly464=) AND not specified
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 7, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000516271.9
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)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024