Canonical Allele Identifier: PA2830123816
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala377Val
CA341585
NM_033508.3:c.1130C>T