Canonical Allele Identifier: PA2830122168
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1098819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.His381Pro
CA367398780
NM_033507.3:c.1142A>C