Canonical Allele Identifier: PA2827936415
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp42His
CA367403461
NM_001354800.1:c.124G>C