Canonical Allele Identifier: PA2825836592
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315034
ClinVar RCV Id: RCV001773228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.His408Gln
CA338254705
NM_001141974.3:c.1224C>G
CA338254706
NM_001141974.3:c.1224C>A