Canonical Allele Identifier: PA2825836239
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1448467
ClinVar RCV Id: RCV001997137
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Arg129Gln
CA637655
NM_001141974.3:c.386G>A