Canonical Allele Identifier: PA2579982470
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg43Cys
CA367403451
NM_000162.5:c.127C>T