Canonical Allele Identifier: PA2830123795
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ser374Phe
CA213713
NM_033508.3:c.1121C>T