Canonical Allele Identifier: PA2825835967
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2183026
ClinVar RCV Id: RCV002592318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Met1128Ile
CA338232677
NM_001141973.3:c.3384G>T
CA338232680
NM_001141973.3:c.3384G>C
CA338232681
NM_001141973.3:c.3384G>A