{{Rsnum
|rsid=386833987
|Chromosome=6
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TA)
|geno3=(TA;TA)
|Gene=SLC17A5
|position=73615418
|Gene_s=SLC17A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=6
|CLNACC=RCV000049964.1
|CLNALLE=1
|CLNDBN=Salla disease
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1470:C1096903:604369:834:87074006
|CLNHGVS=NC_000006.11:g.74325141_74325142delTA
|CLNSIG=4
|Disease=Salla disease
|FwdREF=TA
|REF=CTA
|RSPOS=74325140
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833987
|GENEINFO=SLC17A5:26503
|GENE_ID=26503
|GENE_NAME=SLC17A5
}}{{PMID Auto
|PMID=10947946
|Title=The spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation.
|OA=1
}}

{{PMID Auto
|PMID=11992753
|Title=Phenotypic spectrum of Salla disease, a free sialic acid storage disorder.
}}