Allele Registry

Canonical Allele Identifier: PA110192

Gene: ATP1A2 HGNC NCBI

ClinVar RCV:

RCV000013782

ClinVar Variation:

12919

HGVS (amino-acid)	Matching Registered Transcripts
NP_000693.1:p.Met731Thr	CA256631 NM_000702.4:c.2192T>C