AP1S3 (NM_001039569.2) sequence variants

Editor(s): Francesca CAPON   

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General web sites
DNA NC_000002.12 GRCh38.p13 ENSG00000152056 GRCh38.p13
  NC_000002.11 GRCh37.p13 ENSG00000152056 GRCh37.p13
mRNA NM_001039569.2 ENST00000396654.7
CCDS CCDS42827.1  
Protein NP_001034658.1 ENSP00000379891.2
NCBI Gene 130340  
OMIM Gene 615781  
OMIM Disease    
Nomenclature HGNC  

PubMed of the initial paper:

Other links: