Canonical Allele Identifier: PA2830123815
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala377Asp
CA367398804
NM_033508.3:c.1130C>A