Allele Registry

Canonical Allele Identifier: PA2826305960

Gene: NUP93 HGNC NCBI

ClinVar RCV:

RCV000210563

RCV001799635

RCV001849346

ClinVar Variation:

224964

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229725.1:p.Gly468Val	CA357847 NM_001242796.2:c.1403G>T