Canonical Allele Identifier: PA2825837364
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492619
ClinVar RCV Id: RCV001981097
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Arg1036Ser
CA338232606
NM_001141974.3:c.3106C>A