Canonical Allele Identifier: PA2830122986
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu121Ile
CA367402232
NM_033508.3:c.361C>A