Canonical Allele Identifier: PA2830122443
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_277042.1:p.Ser434_Thr438del
CA2697557239
NM_033507.3:c.1300_1314del