Allele Registry

Canonical Allele Identifier: PA2830123841

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV002281721

ClinVar Variation:

36178

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Met380Arg	CA213719 NM_033508.3:c.1139T>G