Canonical Allele Identifier: PA2825836453
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 209136
ClinVar RCV Id: RCV000191065 RCV002514094
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Gly310Arg
CA276126
NM_001141974.3:c.928G>A
CA338257126
NM_001141974.3:c.928G>C