Canonical Allele Identifier: PA2825835303
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2107180
ClinVar RCV Id: RCV003045561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.His419Gln
CA338254417
NM_001141973.3:c.1257C>G
CA338254421
NM_001141973.3:c.1257C>A