Canonical Allele Identifier: PA2827937204
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.His79Pro
CA367398218
NM_001354801.1:c.236A>C