Canonical Allele Identifier: PA2830122785
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 419624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Val61Met
CA16618472
NM_033508.3:c.181G>A