Canonical Allele Identifier: PA093063
Gene: UBQLN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29952
ClinVar RCV Id: RCV000022844

Amino-acid Alleles

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