Canonical Allele Identifier: PA2830123128
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1741488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe151Ser
CA367401925
NM_033508.3:c.452T>C