Allele Registry

Canonical Allele Identifier: PA2830123821

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000518241

RCV003318500

ClinVar Variation:

447382

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Ala378Gly	CA367398793 NM_033508.3:c.1133C>G