Canonical Allele Identifier: PA2830124094
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val454Met
CA257432
NM_033508.3:c.1360G>A