Canonical Allele Identifier: PA152960
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_000153.1:p.Glu236Lys
CA152959
NM_000162.5:c.706G>A