Canonical Allele Identifier: PA2830123374
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136522
ClinVar RCV Id: RCV003037218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asp204Tyr
CA367401348
NM_033508.3:c.610G>T