Canonical Allele Identifier: PA2579981782
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 522504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp124Val
CA367402205
NM_000162.5:c.371A>T