Canonical Allele Identifier: PA2825837338
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1380896
ClinVar RCV Id: RCV001921821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135446.1:p.Val1021Leu
CA18625653
NM_001141974.3:c.3061G>T
CA338233416
NM_001141974.3:c.3061G>C