Canonical Allele Identifier: PA2827937320
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2734988

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Val32Ala
CA367398281
NM_001354802.1:c.95T>C