Canonical Allele Identifier: PA2830123899
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2581305
ClinVar RCV Id: RCV003331710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg391Ser
CA367398628
NM_033508.3:c.1171C>A