Canonical Allele Identifier: PA2830123553
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435302
ClinVar RCV Id: RCV000501758 RCV001562849 RCV002282182
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala258Thr
CA367400584
NM_033508.3:c.772G>A