Canonical Allele Identifier: PA2827937298
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg17Leu
CA341587
NM_001354802.1:c.50G>T