Allele Registry

Canonical Allele Identifier: PA2826866059

Gene: USP30 HGNC NCBI

ClinVar RCV:

RCV004089151

ClinVar Variation:

2226272

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288104.1:p.Thr304Met	CA6772031 NM_001301175.2:c.911C>T