Allele Registry

Canonical Allele Identifier: PA645460198

Gene: GCK HGNC NCBI

ClinVar Allele:

44896

ClinVar RCV:

RCV000029895

RCV002463602

RCV003883123

ClinVar Variation:

36232

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Met203Val	CA213808 NM_033507.3:c.607A>G