Allele Registry

Canonical Allele Identifier: PA103098

Gene: ATP2A2 HGNC NCBI

ClinVar RCV:

RCV000019377

RCV001650836

ClinVar Variation:

17799

HGVS (amino-acid)	Matching Registered Transcripts
NP_733765.1:p.Pro602Leu	CA127427 NM_170665.4:c.1805C>T