Canonical Allele Identifier: PA2827937300
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2121221
ClinVar RCV Id: RCV003049053
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Val21Ile
CA4239414
NM_001354802.1:c.61G>A