Canonical Allele Identifier: PA2499252076
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 997872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Thr57Pro
CA367397086
NM_001354802.1:c.169A>C