Canonical Allele Identifier: PA2827937130
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709202
ClinVar RCV Id: RCV002289017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Cys45Ser
CA367398745
NM_001354801.1:c.134G>C
CA367398756
NM_001354801.1:c.133T>A