Canonical Allele Identifier: PA2830123878
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu385Pro
CA213723
NM_033508.3:c.1154T>C