P47H (p.Pro47His) variant of MYPN (Myopalladin)
P47H (p.Pro47His) 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.
P47H (p.Pro47His) variant details
- p.Pro47His
- rs777446804
- ClinGen CA377103688
- ClinVar RCV004519864
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available