Canonical Allele Identifier: PA645460241
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr229Met
CA260620
NM_033507.3:c.686C>T