Canonical Allele Identifier: PA2499295135
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1077171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Phe134Leu
CA367402113
NM_033507.3:c.402C>G
CA367402115
NM_033507.3:c.402C>A
CA367402122
NM_033507.3:c.400T>C