Canonical Allele Identifier: PA891855238
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val63Ala
CA367403278
NM_033507.3:c.188T>C