P11T (p.Pro11Thr) variant of SCN1A (P35498)
P11T (p.Pro11Thr) in SCN1A (P35498) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
P11T (p.Pro11Thr) variant details
- p.Pro11Thr
- Ensembl rs1684706255
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available