Allele Registry

Canonical Allele Identifier: PA213726

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029844

RCV003883122

ClinVar Variation:

36181

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Ala387Glu	CA213725 NM_000162.5:c.1160C>A