S3N (p.Ser3Asn) variant of FGFR2 (P21802)
S3N (p.Ser3Asn) in FGFR2 (P21802) is a missense change. The record also includes structural context.
S3N (p.Ser3Asn) variant details
- p.Ser3Asn
- TOPMed rs1271629959
- Missense
- Structural context available
S3N (p.Ser3Asn) in FGFR2 (P21802) is a missense change. The record also includes structural context.