Allele Registry

Canonical Allele Identifier: PA2827936932

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003397220

ClinVar Variation:

2628365

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Ala378Pro	CA367398808 NM_001354800.1:c.1132G>C