Canonical Allele Identifier: PA2830122660
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691828
ClinVar RCV Id: RCV003494025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gln37Leu
CA367403522
NM_033508.3:c.110A>T