H21N (p.His21Asn) variant of PIM1 (P11309)
H21N (p.His21Asn) in PIM1 (P11309) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H21N (p.His21Asn) variant details
- p.His21Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available