Canonical Allele Identifier: PA2827936600
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser174Leu
CA367401688
NM_001354800.1:c.521C>T