Canonical Allele Identifier: PA2830123412
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16144
ClinVar RCV Id: RCV000017526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Tyr213Cys
CA257435
NM_033508.3:c.638A>G