Canonical Allele Identifier: PA2830069341
Gene: ATP13A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3131432
ClinVar RCV Id: RCV004425812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115655.2:p.Thr323Ile
CA355784049
NM_032279.4:c.968C>T