Allele Registry

Canonical Allele Identifier: PA093052

Gene: UBQLN2 HGNC NCBI

ClinVar RCV:

RCV000022843

ClinVar Variation:

29951

HGVS (amino-acid)	Matching Registered Transcripts
NP_038472.2:p.Pro497Ser	CA259705 NM_013444.4:c.1489C>T