Canonical Allele Identifier: PA2580447971
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2075463
ClinVar RCV Id: RCV002967745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Ser409Arg
CA338254785
NM_022089.4:c.1227C>G
CA338254787
NM_022089.4:c.1227C>A
CA338254793
NM_022089.4:c.1225A>C