Canonical Allele Identifier: PA2825835086
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 579095
ClinVar RCV Id: RCV000702289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Arg129Trp
CA338263429
NM_001141973.3:c.385C>T