Canonical Allele Identifier: PA2579979291
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.His156Tyr
CA367401892
NM_000162.5:c.466C>T