Canonical Allele Identifier: PA2830122229
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3024417
ClinVar RCV Id: RCV003883453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala388Thr
CA367398695
NM_033507.3:c.1162G>A