S13A (p.Ser13Ala) variant of MYPN (Myopalladin)
S13A (p.Ser13Ala) in MYPN (Myopalladin) is a missense change. The record also includes structural context.
S13A (p.Ser13Ala) variant details
- p.Ser13Ala
- ExAC rs772628299
- TOPMed rs772628299
- gnomAD rs772628299
- Missense
- Structural context available