Canonical Allele Identifier: PA645460216
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16144
ClinVar RCV Id: RCV000017526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Tyr215Cys
CA257435
NM_033507.3:c.644A>G