Allele Registry

Canonical Allele Identifier: PA288593

Gene: BRIP1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000116156

RCV000212334

RCV000410562

RCV000411633

RCV000587193

RCV000989979

RCV001080937

RCV001354736

RCV001998437

RCV004529953

ClinVar Variation:

128187

1477741

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Glu1126Asp	CA288591 NM_032043.3:c.3378A>C CA400478859 NM_032043.3:c.3378A>T