Canonical Allele Identifier: PA2825836596
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1163729
ClinVar RCV Id: RCV001509025 RCV001821804 RCV001859353 RCV002384858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Arg410Trp
CA637305
NM_001141974.3:c.1228C>T