Allele Registry

Canonical Allele Identifier: PA298827

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000160319

RCV000212323

RCV000477092

RCV000663309

RCV000781178

RCV001194708

RCV003315951

ClinVar Variation:

182330

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Lys797Arg	CA298825 NM_032043.3:c.2390A>G