Allele Registry

Canonical Allele Identifier: PA2830122646

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029836

ClinVar Variation:

36173

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Arg35Pro	CA213709 NM_033508.3:c.104G>C