Canonical Allele Identifier: PA2580490708
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1802664
ClinVar RCV Id: RCV002465951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg47Lys
CA367403428
NM_033507.3:c.140G>A