Canonical Allele Identifier: PA645460252
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129146
ClinVar RCV Id: RCV000117134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu237Lys
CA152959
NM_033507.3:c.709G>A