Canonical Allele Identifier: PA2825837051
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 875293
ClinVar RCV Id: RCV001099008 RCV001856341 RCV004032046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Arg809His
CA636784
NM_001141974.3:c.2426G>A