Canonical Allele Identifier: PA2830123262
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2664850
ClinVar RCV Id: RCV003447825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu184Pro
CA367401583
NM_033508.3:c.551T>C