Canonical Allele Identifier: PA2825836057
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 642673
ClinVar RCV Id: RCV000796179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Leu1174Ter
CA915941146
NM_001141973.3:c.3520del