Canonical Allele Identifier: PA2825836621
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2053515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Arg444Gln
CA637259
NM_001141974.3:c.1331G>A