Canonical Allele Identifier: PA2579981110
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 420070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gln38Pro
CA16618475
NM_000162.5:c.113A>C