Canonical Allele Identifier: PA645459545
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala189Val
CA213802
NM_033507.3:c.566C>T