Canonical Allele Identifier: PA2825836635
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 588886
ClinVar RCV Id: RCV000805500 RCV002315380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Val462Met
CA637215
NM_001141974.3:c.1384G>A