Canonical Allele Identifier: PA645460201
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met203Thr
CA213810
NM_033507.3:c.608T>C