TNFAIP3 (NM_006290.4) sequence variants
(A20, AISBL, OTUD7C, TNFA1P2)

General web sites
DNA	NC_000006.12 GRCh38.p13	ENSG00000118503 GRCh38.p13
	NC_000006.11 GRCh37.p13	ENSG00000118503 GRCh37.p13
	NG_032761.1
mRNA	NM_006290.4
CCDS	CCDS5187.1
Protein	NP_006281.1
NCBI Gene	7128
OMIM Gene	191163
OMIM Disease	616744
Nomenclature	HGNC

PubMed of the initial paper: Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease. Zhou Q & al
Variants review: Association of Clinical Phenotypes in Haploinsufficiency A20 (HA20) With Disrupted Domains of A20 Chen Y & al Autosomic dominant familial Behçet disease and haploinsufficiency A20: A review of the literature Berteau F & al
Other links: MAP VIEW ORPHANET: Orphan disease database