Canonical Allele Identifier: PA2827936417
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585911
ClinVar RCV Id: RCV000711761 RCV003325972 RCV002285407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg43Cys
CA367403451
NM_001354800.1:c.127C>T