Canonical Allele Identifier: PA658819785
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 522504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp125Val
CA367402205
NM_033507.3:c.374A>T