Canonical Allele Identifier: PA2830123787
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Cys370Trp
CA367398928
NM_033508.3:c.1110C>G