Canonical Allele Identifier: PA2580447976
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2107180
ClinVar RCV Id: RCV003045561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.His424Gln
CA338254417
NM_022089.4:c.1272C>G
CA338254421
NM_022089.4:c.1272C>A