Canonical Allele Identifier: PA2579976220
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024419
ClinVar RCV Id: RCV003883455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser383Thr
CA367398738
NM_000162.5:c.1147T>A