Canonical Allele Identifier: PA2579982996
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala208Val
CA4239569
NM_000162.5:c.623C>T