Canonical Allele Identifier: PA645459506
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Thr50Asn
CA213765
NM_033507.3:c.149C>A