Canonical Allele Identifier: PA2825836633
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1900813
ClinVar RCV Id: RCV002571148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Val462Glu
CA637214
NM_001141974.3:c.1385T>A