Canonical Allele Identifier: PA2580490771
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1741488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe153Ser
CA367401925
NM_033507.3:c.458T>C