Canonical Allele Identifier: PA128498
Gene: ATP2A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 29610
ClinVar RCV Id: RCV000022449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001672.1:p.Ala698Val
CA128497
NM_001681.4:c.2093C>T