Canonical Allele Identifier: PA2827937017
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.His416Arg
CA367398216
NM_001354800.1:c.1247A>G