Canonical Allele Identifier: PA645461086
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ile437Asn
CA213751
NM_033507.3:c.1310T>A