Canonical Allele Identifier: PA2830122256
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 981653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met394Thr
CA367398600
NM_033507.3:c.1181T>C