Canonical Allele Identifier: PA2830122465
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 997872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr438Pro
CA367397086
NM_033507.3:c.1312A>C