Canonical Allele Identifier: PA2830123703
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338573
ClinVar RCV Id: RCV001817944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu308Pro
CA367400002
NM_033508.3:c.923T>C