Canonical Allele Identifier: PA658668970
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Trp168Arg
CA367401768
NM_033507.3:c.502T>C
CA367401770
NM_033507.3:c.502T>A