Canonical Allele Identifier: PA2830123784
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807280
ClinVar RCV Id: RCV002475237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala369Pro
CA367398963
NM_033508.3:c.1105G>C