Canonical Allele Identifier: PA2827936516
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 522504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asp124Val
CA367402205
NM_001354800.1:c.371A>T