Allele Registry

Canonical Allele Identifier: PA2741997552

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003327892

ClinVar Variation:

2579457

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Asp206His	CA367401349 NM_033507.3:c.616G>C