Canonical Allele Identifier: PA2741997499
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ser175Leu
CA367401688
NM_033507.3:c.524C>T