Canonical Allele Identifier: PA2825836638
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293791
ClinVar RCV Id: RCV002392825 RCV001753750 RCV002494909 RCV000269192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Pro469Ala
CA637211
NM_001141974.3:c.1405C>G