D33N (p.Asp33Asn) variant of MEN1 (Menin)
D33N (p.Asp33Asn) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as likely pathogenic. The record also includes structural context.
D33N (p.Asp33Asn) variant details
- p.Asp33Asn
- Ensembl rs2136194342
- Likely pathogenic
- Missense
- EBI: Likely pathogenic
- UniProt: Likely pathogenic
- Structural context available