Canonical Allele Identifier: PA645461067
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala388Glu
CA213725
NM_033507.3:c.1163C>A