Canonical Allele Identifier: PA2825835285
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 806073
ClinVar RCV Id: RCV000993929 RCV001644884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Thr397Met
CA637314
NM_001141973.3:c.1190C>T