Allele Registry

Canonical Allele Identifier: PA2827937149

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029844

RCV003883122

ClinVar Variation:

36181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Ala50Glu	CA213725 NM_001354801.1:c.149C>A