Allele Registry

Canonical Allele Identifier: PA2830122125

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003397220

ClinVar Variation:

2628365

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Ala379Pro	CA367398808 NM_033507.3:c.1135G>C