Canonical Allele Identifier: PA2830123072
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 451690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Lys142Leu
CA658655971
NM_033508.3:c.424_425delinsCT