Canonical Allele Identifier: PA2830123138
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700679
ClinVar RCV Id: RCV002285557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val153Ala
CA367401909
NM_033508.3:c.458T>C