Canonical Allele Identifier: PA2827937082
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Leu18Pro
CA367399180
NM_001354801.1:c.53T>C