Canonical Allele Identifier: PA2741997484
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2580878
ClinVar RCV Id: RCV003330073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Lys162Arg
CA367401831
NM_033507.3:c.485A>G