Canonical Allele Identifier: PA645460727
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ser376Phe
CA213713
NM_033507.3:c.1127C>T