Canonical Allele Identifier: PA2830123811
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg376His
CA213715
NM_033508.3:c.1127G>A