Canonical Allele Identifier: PA645406772
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_071372.1:p.Pro474Ala
CA637211
NM_022089.4:c.1420C>G