Canonical Allele Identifier: PA2830123153
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.His155Tyr
CA367401892
NM_033508.3:c.463C>T