Canonical Allele Identifier: PA2827936935
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala379Val
CA367398790
NM_001354800.1:c.1136C>T