Canonical Allele Identifier: PA2829966071
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1912256
ClinVar RCV Id: RCV002600739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Arg1150Trp
CA636480
NM_022089.4:c.3448C>T