Figure 2
From: Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis
Genomic context and evolutionary conservation of NLRP1 homozygous variant identified in primary NLRP1 family 1 (Fig. 2). Variant affects amino acid position 578 in NLRP1 gene evolutionarily invariant in all mammal datasets in the UCSC Genome Browser conservation chain.
