Canonical Allele Identifier: PA2830123119
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe149Ser
CA213784
NM_033508.3:c.446T>C