Canonical Allele Identifier: PA2580447991
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1900813
ClinVar RCV Id: RCV002571148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Val467Glu
CA637214
NM_022089.4:c.1400T>A