Allele Registry

Canonical Allele Identifier: PA2827936721

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029911

RCV003556090

ClinVar Variation:

36248

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Met235Thr	CA213834 NM_001354800.1:c.704T>C