Canonical Allele Identifier: PA2579983049
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136524
ClinVar RCV Id: RCV003037220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala176Thr
CA367401678
NM_000162.5:c.526G>A