Canonical Allele Identifier: PA658668999
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala209Val
CA4239569
NM_033507.3:c.626C>T