Allele Registry

Canonical Allele Identifier: PA195349

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

185300

ClinVar RCV:

RCV000166239

RCV000205783

RCV000217577

RCV001194200

RCV003462205

ClinVar Variation:

186617

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.His213Arg	CA195347 NM_032043.3:c.638A>G