Allele Registry

Canonical Allele Identifier: PA104932

Gene: ATP2A1 HGNC NCBI

ClinVar RCV:

RCV000019384

ClinVar Variation:

17806

HGVS (amino-acid)	Matching Registered Transcripts
NP_775293.1:p.Pro789Leu	CA127438 NM_173201.5:c.2366C>T