Canonical Allele Identifier: PA2827937285
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg12Leu
CA213733
NM_001354802.1:c.35G>T