Allele Registry

Canonical Allele Identifier: PA2827937118

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003397220

ClinVar Variation:

2628365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Ala41Pro	CA367398808 NM_001354801.1:c.121G>C