Canonical Allele Identifier: PA2830122627
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1172675
ClinVar RCV Id: RCV001526668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Glu27Lys
CA367403690
NM_033508.3:c.79G>A