Canonical Allele Identifier: PA2830123842
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709202
ClinVar RCV Id: RCV002289017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Cys381Ser
CA367398745
NM_033508.3:c.1142G>C
CA367398756
NM_033508.3:c.1141T>A