Canonical Allele Identifier: PA2579980669
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2581125
ClinVar RCV Id: RCV003330367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Cys382Gly
CA367398753
NM_000162.5:c.1144T>G