Canonical Allele Identifier: PA2830124006
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700675

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg421Trp
CA367397271
NM_033508.3:c.1261C>T