Canonical Allele Identifier: PA916039356
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Leu6Pro
CA213723
NM_001354802.1:c.17T>C