Canonical Allele Identifier: PA2580448133
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2078375
ClinVar RCV Id: RCV002988600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Pro1080His
CA636540
NM_022089.4:c.3239C>A