NM_000352.6(ABCC8):c.354C>T (p.Val118=) AND Hereditary hyperinsulinism
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001272248.2
Allele description [Variation Report for NM_000352.6(ABCC8):c.354C>T (p.Val118=)]
NM_000352.6(ABCC8):c.354C>T (p.Val118=)
Condition(s)
- Name:
- Hereditary hyperinsulinism
- Identifiers:
Assertion and evidence details
Last Updated: Apr 15, 2024