Allele Registry

Canonical Allele Identifier: PA2827936920

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029838

RCV002463593

ClinVar Variation:

36175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Ser375Phe	CA213713 NM_001354800.1:c.1124C>T