Canonical Allele Identifier: PA2741868018
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2571643
ClinVar RCV Id: RCV003313353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Phe58del
CA2017997767
NM_001354802.1:c.172_174del