Canonical Allele Identifier: PA2741997536
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3026940
ClinVar RCV Id: RCV003887333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp199Ala
CA367401419
NM_033507.3:c.596A>C