Canonical Allele Identifier: PA2830123822
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala378Val
CA367398790
NM_033508.3:c.1133C>T