Canonical Allele Identifier: PA2827936795
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3230479
ClinVar RCV Id: RCV004520630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Tyr273Cys
CA367400492
NM_001354800.1:c.818A>G