Allele Registry

Canonical Allele Identifier: PA2580484692

Gene: USP30 HGNC NCBI

ClinVar RCV:

RCV004089151

ClinVar Variation:

2226272

HGVS (amino-acid)	Matching Registered Transcripts
NP_116052.2:p.Thr335Met	CA6772031 NM_032663.5:c.1004C>T