Canonical Allele Identifier: PA2827936958
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu386Pro
CA213723
NM_001354800.1:c.1157T>C