Allele Registry

Canonical Allele Identifier: PA357851

Gene: NUP93 HGNC NCBI

ClinVar RCV:

RCV000210641

RCV001328162

RCV001532324

RCV003417761

ClinVar Variation:

224968

HGVS (amino-acid)	Matching Registered Transcripts
NP_055484.3:p.Arg388Trp	CA357850 NM_014669.5:c.1162C>T