Canonical Allele Identifier: PA645459519
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe151Ser
CA213784
NM_033507.3:c.452T>C