G56W (p.Gly56Trp) variant of MYPN (Myopalladin)
G56W (p.Gly56Trp) in MYPN (Myopalladin) is a missense change. The record also includes structural context.
G56W (p.Gly56Trp) variant details
- p.Gly56Trp
- cosmic curated COSV10059
- Missense
- Structural context available