Canonical Allele Identifier: PA658668977
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 450644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala177Glu
CA367401673
NM_033507.3:c.530C>A