Canonical Allele Identifier: PA2741837477
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3027054
ClinVar RCV Id: RCV003887447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.His1097Arg
CA18624483
NM_001141974.3:c.3290A>G