Canonical Allele Identifier: PA2827936983
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1978447
ClinVar RCV Id: RCV002750992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Glu395Gly
CA4239419
NM_001354800.1:c.1184A>G