Canonical Allele Identifier: PA2830121992
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 987827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg346Gly
CA367399354
NM_033507.3:c.1036C>G