Canonical Allele Identifier: PA2830122391
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.His417Arg
CA367398216
NM_033507.3:c.1250A>G