Allele Registry

Canonical Allele Identifier: PA288581

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000116152

RCV000206801

RCV000212333

RCV000662500

RCV000781175

RCV003315656

ClinVar Variation:

128183

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Arg1035His	CA288579 NM_032043.3:c.3104G>A