Canonical Allele Identifier: PA2579982881
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg275Cys
CA4239519
NM_000162.5:c.823C>T