Canonical Allele Identifier: PA2579982056
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg377Cys
CA367398826
NM_000162.5:c.1129C>T