Allele Registry

Canonical Allele Identifier: PA645460250

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029911

RCV003556090

ClinVar Variation:

36248

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Met236Thr	CA213834 NM_033507.3:c.707T>C