Allele Registry

Canonical Allele Identifier: PA110213

Gene: ATP1A2 HGNC NCBI

ClinVar RCV:

RCV000013781

RCV001533155

ClinVar Variation:

12918

HGVS (amino-acid)	Matching Registered Transcripts
NP_000693.1:p.Trp887Arg	CA256629 NM_000702.4:c.2659T>C CA343252149 NM_000702.4:c.2659T>A