Canonical Allele Identifier: PA2827937125
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1098819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.His43Pro
CA367398780
NM_001354801.1:c.128A>C