Canonical Allele Identifier: PA2827936643
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447409

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met197Thr
CA367401431
NM_001354800.1:c.590T>C