N51D (p.Asn51Asp) variant of MEN1 (Menin)
N51D (p.Asn51Asp) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
N51D (p.Asn51Asp) variant details
- p.Asn51Asp
- Ensembl rs902475323
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available