Canonical Allele Identifier: PA2579982567
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2734991

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg397Cys
CA4239418
NM_000162.5:c.1189C>T