Canonical Allele Identifier: PA645459493
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 235097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu31Pro
CA10581225
NM_033507.3:c.92T>C