Canonical Allele Identifier: PA2825835972
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492619
ClinVar RCV Id: RCV001981097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Ser1131Arg
CA338232604
NM_001141973.3:c.3393C>G
CA338232606
NM_001141973.3:c.3393C>A
CA338232617
NM_001141973.3:c.3391A>C