Canonical Allele Identifier: PA2580490757
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136527
ClinVar RCV Id: RCV003060108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.His138Arg
CA367402077
NM_033507.3:c.413A>G