Allele Registry

Canonical Allele Identifier: PA645460206

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000117132

RCV000497903

RCV001844042

RCV003343641

ClinVar Variation:

129145

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Thr207Pro	CA152955 NM_033507.3:c.619A>C