Canonical Allele Identifier: PA2825835320
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2053515
ClinVar RCV Id: RCV002922563 RCV002922564 RCV003491168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Arg444Gln
CA637259
NM_001141973.3:c.1331G>A