Canonical Allele Identifier: PA2825835895
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2044385
ClinVar RCV Id: RCV002903650 RCV003274071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135445.1:p.Ala1064Gly
CA18625642
NM_001141973.3:c.3191C>G