Canonical Allele Identifier: PA2830123442
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 546098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ile224Met
CA367401129
NM_033508.3:c.672C>G