Allele Registry

Canonical Allele Identifier: PA2830123315

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003887333

ClinVar Variation:

3026940

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Asp197Ala	CA367401419 NM_033508.3:c.590A>C