Canonical Allele Identifier: PA2826305840
Gene: NUP93 HGNC NCBI

Linked Data

ClinVar Variation Id: 224964
ClinVar RCV Id: RCV000210563 RCV001799635 RCV001849346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229724.1:p.Gly468Val
CA357847
NM_001242795.2:c.1403G>T