Canonical Allele Identifier: PA658807819
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 498321
ClinVar RCV Id: RCV000593522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.His413Tyr
CA338254714
NM_022089.4:c.1237C>T