Canonical Allele Identifier: PA2830122039
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807280
ClinVar RCV Id: RCV002475237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala371Pro
CA367398963
NM_033507.3:c.1111G>C