{{Rsnum
|rsid=386833681
|Chromosome=3
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=AMT
|position=49421573
|Gene_s=AMT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=3
|CLNACC=RCV000049642.1
|CLNALLE=1
|CLNDBN=Non-ketotic hyperglycinemia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1357:C0751748:605899:407:237939006
|CLNHGVS=NC_000003.11:g.49459006C>G
|CLNSIG=4
|Disease=Non-ketotic hyperglycinemia
|FwdALT=C
|FwdREF=G
|REF=C
|RSPOS=49459006
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833681
|GENEINFO=AMT:275
|GENE_ID=275
|GENE_NAME=AMT
}}{{PMID Auto
|PMID=19299230
|Title=Atypical glycine encephalopathy in an extremely low birth weight infant: description of a new mutation and clinical and electroencephalographic analysis.
}}