Canonical Allele Identifier: PA2830122056
Gene: GCK HGNC NCBI
ClinVar RCV:
RCV003326073
ClinVar Variation:
2578347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Cys372Tyr
CA367398935
NM_033507.3:c.1115G>A