Canonical Allele Identifier: PA645461080
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg398Leu
CA341587
NM_033507.3:c.1193G>T