Canonical Allele Identifier: PA2830123863
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024418
ClinVar RCV Id: RCV003883454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ser382Trp
CA367398735
NM_033508.3:c.1145C>G