Canonical Allele Identifier: PA2830122984
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735019

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu121Pro
CA367402227
NM_033508.3:c.362T>C