Canonical Allele Identifier: PA2827937200
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Lys77Glu
CA213739
NM_001354801.1:c.229A>G