Allele Registry

Canonical Allele Identifier: PA2741868034

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003397220

ClinVar Variation:

2628365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Ala56Pro	CA367398808 NM_001354803.2:c.166G>C