Canonical Allele Identifier: PA2573095136
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315034
ClinVar RCV Id: RCV001773228

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.His413Gln
CA338254705
NM_022089.4:c.1239C>G
CA338254706
NM_022089.4:c.1239C>A