Canonical Allele Identifier: PA2827937242
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ser116Leu
CA213760
NM_001354801.1:c.347C>T