Canonical Allele Identifier: PA2825835302
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293794
ClinVar RCV Id: RCV000291316 RCV001243069 RCV002392826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Arg410Gln
CA637304
NM_001141973.3:c.1229G>A