Canonical Allele Identifier: PA2827936622
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu185Arg
CA367401582
NM_001354800.1:c.554T>G