Canonical Allele Identifier: PA2580490788
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136524
ClinVar RCV Id: RCV003037220

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala177Thr
CA367401678
NM_033507.3:c.529G>A