Canonical Allele Identifier: PA2579976238
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2767216
ClinVar RCV Id: RCV003573794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser375Tyr
CA367398843
NM_000162.5:c.1124C>A