Canonical Allele Identifier: PA2826305842
Gene: NUP93 HGNC NCBI

Linked Data

ClinVar Variation Id: 635548
ClinVar RCV Id: RCV000787021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229724.1:p.Ala490Pro
CA395993090
NM_001242795.2:c.1468G>C