Canonical Allele Identifier: PA2829966069
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1420889
ClinVar RCV Id: RCV001923609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Arg1148Cys
CA636482
NM_022089.4:c.3442C>T