Canonical Allele Identifier: PA2830123257
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val180Ala
CA213800
NM_033508.3:c.539T>C