PSMB9 (NM_002800.5) sequence variants
(LMP2, PSMB6i, RING12, beta1i)

General web sites
DNA	NC_000006.12 GRCh38.p13	ENSG00000240065 GRCh38.p13
	NC_000006.11 GRCh37.p13	ENSG00000240065 GRCh37.p13
mRNA	NM_002800.5	ENST00000374859.3
CCDS	CCDS4759.1
Protein	NP_002791.1	ENSP00000363993.2
NCBI Gene	5698
OMIM Gene	177045
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