CRACR2A

calcium release activated channel regulator 2A
OMIM: 614178, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CRACR2A in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 5.3
Latest signed off version: v5.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • late onset combined immunodeficiency