Canonical Allele Identifier: PA2827937292
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1522625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Arg14Leu
CA367398578
NM_001354802.1:c.41G>T