Canonical Allele Identifier: PA645460191
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 431972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile190Thr
CA367401550
NM_033507.3:c.569T>C