Canonical Allele Identifier: PA2580447910
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2439338
ClinVar RCV Id: RCV003143607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Glu118Lys
CA637661
NM_022089.4:c.352G>A