Canonical Allele Identifier: PA2830123792
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val373Met
CA367398877
NM_033508.3:c.1117G>A