Canonical Allele Identifier: PA645460267
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val254Ala
CA213842
NM_033507.3:c.761T>C