Canonical Allele Identifier: PA891855252
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile127Thr
CA367402185
NM_033507.3:c.380T>C