Canonical Allele Identifier: PA2827936549
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Gly147Asp
CA213782
NM_001354800.1:c.440G>A