PSMB4 (NM_002796.3) sequence variants
(HN3, HsN3, PROS26, PROS-26)

General web sites
DNA	NC_000001.11 GRCh38.p13	ENSG00000159377 GRCh38.p13
	NC_000001.10 GRCh37.p13	ENSG00000159377 GRCh37.p13
mRNA	NM_002796.3	ENST00000290541.7
CCDS	CCDS996.1
Protein	NP_002787.2	ENSP00000290541.6
NCBI Gene	5692
OMIM Gene	602177
OMIM Disease	617591
Nomenclature	HGNC

PubMed of the initial paper: Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production. Brehm A & al
Other links: MAP VIEW ORPHANET: Orphan disease database