Canonical Allele Identifier: PA1139748979
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu238Lys
CA367400730
NM_033507.3:c.712G>A