Allele Registry

Canonical Allele Identifier: PA195895

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

185302

ClinVar RCV:

RCV000166445

RCV000461927

ClinVar Variation:

186795

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Asp184Asn	CA195893 NM_032043.3:c.550G>A