Allele Registry

Canonical Allele Identifier: PA2828187077

Gene: ATP2B4 HGNC NCBI

ClinVar RCV:

RCV001884638

RCV004041497

ClinVar Variation:

1393853

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352712.1:p.Pro139Ser	CA1341379 NM_001365783.2:c.415C>T