Canonical Allele Identifier: PA2830123390
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala207Thr
CA367401322
NM_033508.3:c.619G>A