Canonical Allele Identifier: PA2825835291
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2075463
ClinVar RCV Id: RCV002967745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Ser404Arg
CA338254785
NM_001141973.3:c.1212C>G
CA338254787
NM_001141973.3:c.1212C>A
CA338254793
NM_001141973.3:c.1210A>C