Canonical Allele Identifier: PA2825835998
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1383259
ClinVar RCV Id: RCV001892463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Cys1140Tyr
CA636485
NM_001141973.3:c.3419G>A