R32T (p.Arg32Thr) variant of MYPN (Myopalladin)
R32T (p.Arg32Thr) in MYPN (Myopalladin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
R32T (p.Arg32Thr) variant details
- p.Arg32Thr
- rs2495460087
- ClinGen CA377103601
- ClinVar RCV004519893
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available