Canonical Allele Identifier: PA2830123243
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2754882
ClinVar RCV Id: RCV003564073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Glu176Asp
CA367401655
NM_033508.3:c.528A>C
CA367401656
NM_033508.3:c.528A>T