Allele Registry

Canonical Allele Identifier: PA117043

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000005003

RCV000582137

RCV000636166

ClinVar Variation:

4737

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Met299Ile	CA117041 NM_032043.3:c.897G>A CA400484678 NM_032043.3:c.897G>T CA400484679 NM_032043.3:c.897G>C