Canonical Allele Identifier: PA093052
Gene: UBQLN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29951
ClinVar RCV Id: RCV000022843

Amino-acid Alleles

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