Allele Registry

Canonical Allele Identifier: PA645406817

Gene: ATP13A2 HGNC NCBI

ClinVar RCV:

RCV000415585

ClinVar Variation:

374887

HGVS (amino-acid)	Matching Registered Transcripts
NP_071372.1:p.Phe1051del	CA16043958 NM_022089.4:c.3152_3154del