Canonical Allele Identifier: PA2827936920
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser375Phe
CA213713
NM_001354800.1:c.1124C>T