Canonical Allele Identifier: PA2827936815
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2098687
ClinVar RCV Id: RCV003031070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Pro284Leu
CA367400423
NM_001354800.1:c.851C>T