Canonical Allele Identifier: PA2825836219
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1015771
ClinVar RCV Id: RCV001314682
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Ser116Arg
CA338263632
NM_001141974.3:c.348C>A
CA338263633
NM_001141974.3:c.348C>G
CA338263691
NM_001141974.3:c.346A>C