Allele Registry

Canonical Allele Identifier: PA2827331042

Gene: NUP107 HGNC NCBI

ClinVar RCV:

RCV000760138

ClinVar Variation:

619945

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317121.1:p.Cys413Tyr	CA6677751 NM_001330192.2:c.1238G>A