Canonical Allele Identifier: PA2825042275
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp42His
CA367403461
NM_000162.5:c.124G>C