Canonical Allele Identifier: PA2830124005
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1800884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg421Leu
CA157911892
NM_033508.3:c.1262G>T