Allele Registry

Canonical Allele Identifier: PA351657

Gene: ATP1A2 HGNC NCBI

ClinVar RCV:

RCV000207519

ClinVar Variation:

222078

HGVS (amino-acid)	Matching Registered Transcripts
NP_000693.1:p.Val191Met	CA351655 NM_000702.4:c.571G>A