Canonical Allele Identifier: PA2830122704
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585910
ClinVar RCV Id: RCV000711760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg42Ser
CA367403453
NM_033508.3:c.124C>A