Canonical Allele Identifier: PA2825837319
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397253
ClinVar RCV Id: RCV001891662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Ser1011Thr
CA18625726
NM_001141974.3:c.3032G>C