Allele Registry

Canonical Allele Identifier: PA2827936397

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029836

ClinVar Variation:

36173

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Arg36Pro	CA213709 NM_001354800.1:c.107G>C