Canonical Allele Identifier: PA2827937112
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Arg40Cys
CA367398826
NM_001354801.1:c.118C>T