Allele Registry

Canonical Allele Identifier: PA2827936681

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017526

ClinVar Variation:

16144

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Tyr214Cys	CA257435 NM_001354800.1:c.641A>G