Canonical Allele Identifier: PA2580490841
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2098687
ClinVar RCV Id: RCV003031070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Pro285Leu
CA367400423
NM_033507.3:c.854C>T