Canonical Allele Identifier: PA658668948
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 451690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Lys144Leu
CA658655971
NM_033507.3:c.430_431delinsCT