Canonical Allele Identifier: PA645460211
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435303

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile212Asn
CA367401285
NM_033507.3:c.635T>A