Canonical Allele Identifier: PA2827936973
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg392Leu
CA213733
NM_001354800.1:c.1175G>T