Canonical Allele Identifier: PA2580229341
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1727652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg55Ser
CA367398819
NM_001354803.2:c.163C>A