Canonical Allele Identifier: PA2830122686
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp41His
CA367403461
NM_033508.3:c.121G>C