Canonical Allele Identifier: PA2827937137
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024418
ClinVar RCV Id: RCV003883454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ser46Trp
CA367398735
NM_001354801.1:c.137C>G