NM_001370259.2(MEN1):c.*126C>T AND Hyperparathyroidism
- Germline classification:
- Uncertain significance (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:
- RCV001108501.5
Allele description [Variation Report for NM_001370259.2(MEN1):c.*126C>T]
NM_001370259.2(MEN1):c.*126C>T
Condition(s)
- Name:
- Hyperparathyroidism
- Identifiers:
- MONDO: MONDO:0001741; MedGen: C0020502; Human Phenotype Ontology: HP:0000843
-
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Last Updated: Aug 4, 2024