Canonical Allele Identifier: PA2579981779
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972807

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp132Asn
CA4239636
NM_000162.5:c.394G>A