Canonical Allele Identifier: PA2830123812
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg376Cys
CA367398826
NM_033508.3:c.1126C>T