Canonical Allele Identifier: PA357848
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_055484.3:p.Gly591Val
CA357847
NM_014669.5:c.1772G>T