Canonical Allele Identifier: PA2825836607
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 954358
ClinVar RCV Id: RCV001226802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Ala431Thr
CA338254179
NM_001141974.3:c.1291G>A