Allele Registry

Canonical Allele Identifier: PA2826603052

Gene: UBXN8 HGNC NCBI

ClinVar RCV:

RCV004156892

ClinVar Variation:

2314638

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269128.2:p.Gln66Glu	CA370888279 NM_001282199.2:c.196C>G