Allele Registry

Canonical Allele Identifier: PA093063

Gene: UBQLN2 HGNC NCBI

ClinVar Allele:

38907

ClinVar RCV:

RCV000022844

ClinVar Variation:

29952

HGVS (amino-acid)	Matching Registered Transcripts
NP_038472.2:p.Pro506Thr	CA259707 NM_013444.4:c.1516C>A