Canonical Allele Identifier: PA2830123387
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala207Val
CA4239569
NM_033508.3:c.620C>T