NM_001370259.2(MEN1):c.1341T>G (p.Phe447Leu) AND Familial isolated hyperparathyroidism
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 9, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000710034.1
Allele description [Variation Report for NM_001370259.2(MEN1):c.1341T>G (p.Phe447Leu)]
NM_001370259.2(MEN1):c.1341T>G (p.Phe447Leu)
Condition(s)
- Name:
- Familial isolated hyperparathyroidism
- Identifiers:
- MONDO: MONDO:0015027; MedGen: C4551961
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Last Updated: Sep 29, 2024