Canonical Allele Identifier: PA916067038
Gene: ATP13A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 734313
ClinVar RCV Id: RCV000909715 RCV003923129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115655.2:p.Pro1166Leu
CA2757736
NM_032279.4:c.3497C>T