Canonical Allele Identifier: PA645459521
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Pro154Ser
CA213788
NM_033507.3:c.460C>T