Canonical Allele Identifier: PA2830122665
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 420070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gln37Pro
CA16618475
NM_033508.3:c.110A>C