Canonical Allele Identifier: PA645459498
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 420070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gln39Pro
CA16618475
NM_033507.3:c.116A>C