Allele Registry

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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