H46N (p.His46Asn) variant of MEN1 (Menin)
H46N (p.His46Asn) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
H46N (p.His46Asn) variant details
- p.His46Asn
- Ensembl rs2136192749
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available