Canonical Allele Identifier: PA2827936949
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024419
ClinVar RCV Id: RCV003883455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser383Thr
CA367398738
NM_001354800.1:c.1147T>A