Canonical Allele Identifier: PA2830123914
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 981653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met392Thr
CA367398600
NM_033508.3:c.1175T>C