Canonical Allele Identifier: PA2825078429
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2698504
ClinVar RCV Id: RCV003551796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser433_Thr437del
CA2697557239
NM_000162.5:c.1297_1311del