Canonical Allele Identifier: PA645460329
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435305

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu315Pro
CA367399950
NM_033507.3:c.944T>C