{{Rsnum
|rsid=80356676
|Chromosome=1
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=NTRK1
|position=156879176
|Gene_s=NTRK1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80356676
|Reversed=0
|FwdREF=GCC
|FwdALT=T
|REF=C
|ALT=CT
|RSPOS=156879176
|CHROM=1
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168001205000002110200
|GENEINFO=NTRK1:4914
|GENE_NAME=NTRK1
|GENE_ID=4914
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.156879176_156879177insT
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=256800
|CLNDBN=Hereditary insensitivity to pain with anhidrosis
|Tags=PM;PMC;SLO;NSF;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000020469.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1769:C0020074:256800:ORPHA642:62985007
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_001007792.1:c.1752_1753insT; NBK1769
|Disease=Hereditary insensitivity to pain with anhidrosis
}}{{PMID Auto
|PMID=10861667
|Title=Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies.
}}

{{PMID Auto
|PMID=11668614
|Title=Congenital insensitivity to pain with anhidrosis (CIPA): novel mutations of the TRKA (NTRK1) gene, a putative uniparental disomy, and a linkage of the mutant TRKA and PKLR genes in a family with CIPA and pyruvate kinase deficiency.
}}