Canonical Allele Identifier: PA2830122678
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met40Thr
CA16609270
NM_033508.3:c.119T>C