Canonical Allele Identifier: PA2579977108
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233993
ClinVar RCV Id: RCV004527569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe152Ile
CA367401928
NM_000162.5:c.454T>A