Canonical Allele Identifier: PA2827937271
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995100
ClinVar RCV Id: RCV001288973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ala4Pro
CA367398729
NM_001354802.1:c.10G>C