Canonical Allele Identifier: PA2580447972
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1757047
ClinVar RCV Id: RCV002365138

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Leu412Phe
CA338254715
NM_022089.4:c.1236G>T
CA338254716
NM_022089.4:c.1236G>C