Canonical Allele Identifier: PA2580229274
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1800884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg85Leu
CA157911892
NM_001354801.1:c.254G>T