Canonical Allele Identifier: PA2830123534
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735005
ClinVar RCV Id: RCV003555335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr254Ala
CA367400608
NM_033508.3:c.760A>G