Canonical Allele Identifier: PA2573296590
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1679555
ClinVar RCV Id: RCV002227434 RCV002337411 RCV003883190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly176Ala
CA367401681
NM_033507.3:c.527G>C