Canonical Allele Identifier: PA2573182644
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1420889
ClinVar RCV Id: RCV001923609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Pro1047Leu
CA636482
NM_001141974.3:c.3140C>T