Canonical Allele Identifier: PA2830123865
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024419
ClinVar RCV Id: RCV003883455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ser382Thr
CA367398738
NM_033508.3:c.1144T>A