Canonical Allele Identifier: PA2827936687
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36240

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Cys220Tyr
CA213822
NM_001354800.1:c.659G>A