Canonical Allele Identifier: PA645406730
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 293795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Ala403Glu
CA637312
NM_022089.4:c.1208C>A