Canonical Allele Identifier: PA2830122166
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala380Val
CA367398790
NM_033507.3:c.1139C>T