Canonical Allele Identifier: PA2827936760
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735005
ClinVar RCV Id: RCV003555335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Thr255Ala
CA367400608
NM_001354800.1:c.763A>G