Canonical Allele Identifier: PA2579976219
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024418
ClinVar RCV Id: RCV003883454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser383Trp
CA367398735
NM_000162.5:c.1148C>G