Canonical Allele Identifier: PA645461111
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala457Val
CA257433
NM_033507.3:c.1370C>T