H42N (p.His42Asn) variant of ATP1A2 (P50993)
H42N (p.His42Asn) in ATP1A2 (P50993) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
H42N (p.His42Asn) variant details
- p.His42Asn
- NCI-TCGA Cosmic COSV1007
- cosmic curated COSV10076
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available