Canonical Allele Identifier: PA645459518
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly148Asp
CA213782
NM_033507.3:c.443G>A