Canonical Allele Identifier: PA2580447987
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072551
ClinVar RCV Id: RCV002949594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Arg451Trp
CA637257
NM_022089.4:c.1351C>T