Canonical Allele Identifier: PA2827936425
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 429796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu45Pro
CA367403437
NM_001354800.1:c.134T>C