Canonical Allele Identifier: PA096458
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2574158
ClinVar RCV Id: RCV003318523

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr168Pro
CA367401755
NM_000162.5:c.502A>C