N40D (p.Asn40Asp) variant of MYPN (Myopalladin)
N40D (p.Asn40Asp) 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.
N40D (p.Asn40Asp) variant details
- p.Asn40Asp
- rs2495460352
- ClinGen CA377103643
- ClinVar RCV003168450
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available