Canonical Allele Identifier: PA2579982460
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585913
ClinVar RCV Id: RCV000711764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg43Pro
CA367403448
NM_000162.5:c.128G>C