Canonical Allele Identifier: PA2741997567
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2684209
ClinVar RCV Id: RCV003482705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile212Thr
CA367401287
NM_033507.3:c.635T>C