Canonical Allele Identifier: PA2579977518
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2580878
ClinVar RCV Id: RCV003330073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Lys161Arg
CA367401831
NM_000162.5:c.482A>G