Canonical Allele Identifier: PA2573281639
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492619
ClinVar RCV Id: RCV001981097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Ser1136Arg
CA338232604
NM_022089.4:c.3408C>G
CA338232606
NM_022089.4:c.3408C>A
CA338232617
NM_022089.4:c.3406A>C