Canonical Allele Identifier: PA2830124095
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala455Val
CA257433
NM_033508.3:c.1364C>T