Canonical Allele Identifier: PA2825836589
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1757047
ClinVar RCV Id: RCV002365138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Leu407Phe
CA338254715
NM_001141974.3:c.1221G>T
CA338254716
NM_001141974.3:c.1221G>C