Canonical Allele Identifier: PA213817
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36237

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser212del
CA213816
NM_000162.5:c.635_637del