Allele Registry

Canonical Allele Identifier: PA2827937080

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029835

RCV003493414

RCV003556089

ClinVar Variation:

36172

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Ile11Phe	CA213707 NM_001354801.1:c.31A>T