Canonical Allele Identifier: PA2825835343
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352645
ClinVar RCV Id: RCV002039844 RCV003481140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Arg482Gln
CA637201
NM_001141973.3:c.1445G>A