Allele Registry

Canonical Allele Identifier: PA102919

Gene: ATP2A2 HGNC NCBI

ClinVar RCV:

RCV000019370

RCV000493249

RCV002288512

ClinVar Variation:

17792

HGVS (amino-acid)	Matching Registered Transcripts
NP_733765.1:p.Asn767Ser	CA127417 NM_170665.4:c.2300A>G