Canonical Allele Identifier: PA2830122271
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1978447
ClinVar RCV Id: RCV002750992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Glu396Gly
CA4239419
NM_033507.3:c.1187A>G