Canonical Allele Identifier: PA2827937149
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala50Glu
CA213725
NM_001354801.1:c.149C>A