Canonical Allele Identifier: PA2827936383
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36230
ClinVar RCV Id: RCV000029893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ile19Met
CA213804
NM_001354800.1:c.57C>G