N51I (p.Asn51Ile) variant of MEN1 (Menin)
N51I (p.Asn51Ile) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
N51I (p.Asn51Ile) variant details
- p.Asn51Ile
- cosmic curated COSV56340
- Ensembl rs1942010838
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available