Canonical Allele Identifier: PA2827937250
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala119Val
CA257433
NM_001354801.1:c.356C>T