Allele Registry

Canonical Allele Identifier: PA2573296696

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV001942615

ClinVar Variation:

1365290

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Ile226Thr	CA367401133 NM_033507.3:c.677T>C