Canonical Allele Identifier: PA2825835074
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015771
ClinVar RCV Id: RCV001314682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Ser116Arg
CA338263632
NM_001141973.3:c.348C>A
CA338263633
NM_001141973.3:c.348C>G
CA338263691
NM_001141973.3:c.346A>C