Canonical Allele Identifier: PA658807866
Gene: ATP13A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 533805
ClinVar RCV Id: RCV000641066
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071372.1:p.Phe1159Ser
CA338232301
NM_022089.4:c.3476T>C