Allele Registry

Canonical Allele Identifier: PA2827937313

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000516548

RCV004527381

ClinVar Variation:

447386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341731.1:p.Gly30Asp	CA367398309 NM_001354802.1:c.89G>A