Canonical Allele Identifier: PA1139748694
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly69Asp
CA157919943
NM_033507.3:c.206G>A