Canonical Allele Identifier: PA2825835877
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728485
ClinVar RCV Id: RCV002322688
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Leu1054Arg
CA18625694
NM_001141973.3:c.3161T>G