Canonical Allele Identifier: PA2830123193
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 997861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu163Pro
CA367401792
NM_033508.3:c.488T>C