Canonical Allele Identifier: PA2830123434
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136520
ClinVar RCV Id: RCV003060105

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly222Val
CA367401157
NM_033508.3:c.665G>T