Canonical Allele Identifier: PA2827937394
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1489311
ClinVar RCV Id: RCV002001467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.His102Pro
CA367397239
NM_001354803.2:c.305A>C