Canonical Allele Identifier: PA2825835222
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 209136
ClinVar RCV Id: RCV000191065 RCV002514094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Gly310Arg
CA276126
NM_001141973.3:c.928G>A
CA338257126
NM_001141973.3:c.928G>C