Canonical Allele Identifier: PA2830123057
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1803244
ClinVar RCV Id: RCV002466914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe132Val
CA367402121
NM_033508.3:c.394T>G