Canonical Allele Identifier: PA2825835306
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1958487
ClinVar RCV Id: RCV002696109

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Lys422Glu
CA338254367
NM_001141973.3:c.1264A>G