Allele Registry

Canonical Allele Identifier: PA2827936939

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV002281721

ClinVar Variation:

36178

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Met381Arg	CA213719 NM_001354800.1:c.1142T>G