Canonical Allele Identifier: PA891855260
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.His157Tyr
CA367401892
NM_033507.3:c.469C>T