Allele Registry

Canonical Allele Identifier: PA1139728293

Gene: UBQLN2 HGNC NCBI

ClinVar Allele:

861439

ClinVar RCV:

RCV001095427

ClinVar Variation:

873224

HGVS (amino-acid)	Matching Registered Transcripts
NP_038472.2:p.Pro506Ser	CA413380724 NM_013444.4:c.1516C>T