Canonical Allele Identifier: PA2830121881
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233734
ClinVar RCV Id: RCV004526584

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly286Val
CA367400418
NM_033507.3:c.857G>T