Allele Registry

Canonical Allele Identifier: PA270967

Gene: UBQLN2 HGNC NCBI

ClinVar Allele:

167455

ClinVar RCV:

RCV000144928

ClinVar Variation:

157594

HGVS (amino-acid)	Matching Registered Transcripts
NP_038472.2:p.Pro497Leu	CA270965 NM_013444.4:c.1490C>T