Canonical Allele Identifier: PA2830123405
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2684209
ClinVar RCV Id: RCV003482705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ile210Thr
CA367401287
NM_033508.3:c.629T>C