Canonical Allele Identifier: PA891855221
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp43His
CA367403461
NM_033507.3:c.127G>C