Canonical Allele Identifier: PA2830123481
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807281
ClinVar RCV Id: RCV002475238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Glu235Val
CA367400733
NM_033508.3:c.704A>T