Canonical Allele Identifier: PA2825836577
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293795
ClinVar RCV Id: RCV000339348 RCV002519411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Ala398Glu
CA637312
NM_001141974.3:c.1193C>A