Canonical Allele Identifier: PA2830123168
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2700200
ClinVar RCV Id: RCV003547122

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ile158Thr
CA367401855
NM_033508.3:c.473T>C