Canonical Allele Identifier: PA2499288747
Gene: ATP13A2 HGNC NCBI
ClinVar Allele:
1022752
ClinVar RCV:
RCV001350763
ClinVar Variation:
1046235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Val653Ile
CA637026
NM_022089.4:c.1957G>A