Canonical Allele Identifier: PA257434
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala456Val
CA257433
NM_000162.5:c.1367C>T