Canonical Allele Identifier: PA2830122787
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val61Ala
CA367403278
NM_033508.3:c.182T>C