Canonical Allele Identifier: PA2579974346
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val62Ala
CA367403278
NM_000162.5:c.185T>C