Allele Registry

Canonical Allele Identifier: PA2827936650

Gene: GCK HGNC NCBI

ClinVar Allele:

44896

ClinVar RCV:

RCV000029895

RCV002463602

RCV003883123

ClinVar Variation:

36232

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Met202Val	CA213808 NM_001354800.1:c.604A>G