Canonical Allele Identifier: PA2579978851
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.His416Arg
CA367398216
NM_000162.5:c.1247A>G