Canonical Allele Identifier: PA2579982854
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447424
ClinVar RCV Id: RCV000517815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg303Leu
CA367400050
NM_000162.5:c.908G>T