Canonical Allele Identifier: PA2830123987
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.His415Arg
CA367398216
NM_033508.3:c.1244A>G