Canonical Allele Identifier: PA916062734
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 806073
ClinVar RCV Id: RCV000993929 RCV001644884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Thr402Met
CA637314
NM_022089.4:c.1205C>T