Canonical Allele Identifier: PA2579976718
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1741488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe152Ser
CA367401925
NM_000162.5:c.455T>C