Allele Registry

Canonical Allele Identifier: PA645460216

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017526

ClinVar Variation:

16144

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Tyr215Cys	CA257435 NM_033507.3:c.644A>G