Canonical Allele Identifier: PA2827937275
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233999
ClinVar RCV Id: RCV004527575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Leu6Arg
CA367398699
NM_001354802.1:c.17T>G