Allele Registry

Canonical Allele Identifier: PA645459496

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029836

ClinVar Variation:

36173

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Arg37Pro	CA213709 NM_033507.3:c.110G>C