Allele Registry

Canonical Allele Identifier: PA2830123412

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017526

ClinVar Variation:

16144

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Tyr213Cys	CA257435 NM_033508.3:c.638A>G