Canonical Allele Identifier: PA2830122793
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg62Cys
CA4239707
NM_033508.3:c.184C>T