Canonical Allele Identifier: PA1139750767
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 856542
ClinVar RCV Id: RCV001062022 RCV002320317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Ala136Val
CA637652
NM_022089.4:c.407C>T