Canonical Allele Identifier: PA2830123928
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 21077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg396Leu
CA341587
NM_033508.3:c.1187G>T