Allele Registry

Canonical Allele Identifier: PA357848

Gene: NUP93 HGNC NCBI

ClinVar RCV:

RCV000210563

RCV001799635

RCV001849346

ClinVar Variation:

224964

HGVS (amino-acid)	Matching Registered Transcripts
NP_055484.3:p.Gly591Val	CA357847 NM_014669.5:c.1772G>T