Canonical Allele Identifier: PA2825836622
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072551
ClinVar RCV Id: RCV002949594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Arg446Trp
CA637257
NM_001141974.3:c.1336C>T