LACC1 (NM_001128303.2) sequence variants
(FAMIN, C13orf31)

General web sites
DNA	NC_000013.11 GRCh38.p13	ENSG00000179630 GRCh38.p13
	NC_000013.10 GRCh37.p13	ENSG00000179630 GRCh37.p13
	NG_053160.1
mRNA	NM_001128303.2
CCDS	CCDS9391
Protein	NP_001121775.1	ENSP00000391747.1
NCBI Gene	144811
OMIM Gene	613409
OMIM Disease	618795
Nomenclature	HGNC

PubMed of the initial paper: Association of a mutation in LACC1 with a monogenic form of systemic juvenile idiopathic arthritis. Wakil SM & al
Variants review: New or vanishing frontiers: LACC1- associated juvenile arthritis Sulaiman M Al-Mayouf & al
Other links: MAP VIEW ORPHANET: Orphan disease database