Canonical Allele Identifier: PA2830123823
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1098819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.His379Pro
CA367398780
NM_033508.3:c.1136A>C