Allele Registry

Canonical Allele Identifier: PA2826305796

Gene: NUP93 HGNC NCBI

ClinVar RCV:

RCV000210641

RCV001328162

RCV001532324

RCV003417761

ClinVar Variation:

224968

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229724.1:p.Arg265Trp	CA357850 NM_001242795.2:c.793C>T