Allele Registry

Canonical Allele Identifier: PA891850224

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV002313595

RCV002534560

ClinVar Variation:

588656

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Val1049Met	CA636589 NM_022089.4:c.3145G>A