Canonical Allele Identifier: PA2830123586
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu270Pro
CA213854
NM_033508.3:c.809T>C