Canonical Allele Identifier: PA2830123364
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val202Ala
CA367401366
NM_033508.3:c.605T>C