Canonical Allele Identifier: PA2825836014
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1912256
ClinVar RCV Id: RCV002600739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Arg1145Trp
CA636480
NM_001141973.3:c.3433C>T