Canonical Allele Identifier: PA2830123818
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2628365
ClinVar RCV Id: RCV003397220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala377Pro
CA367398808
NM_033508.3:c.1129G>C