Canonical Allele Identifier: PA2827937121
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala42Val
CA367398790
NM_001354801.1:c.125C>T