Canonical Allele Identifier: PA2580229353
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1709202
ClinVar RCV Id: RCV002289017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Cys60Ser
CA367398745
NM_001354803.2:c.179G>C
CA367398756
NM_001354803.2:c.178T>A