Canonical Allele Identifier: PA2827937420
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2701170
ClinVar RCV Id: RCV003549568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Glu121Lys
CA367396999
NM_001354803.2:c.361G>A