Allele Registry

Canonical Allele Identifier: PA645436323

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000233279

RCV001364306

ClinVar Variation:

241659

1055606

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Phe1234Leu	CA10583610 NM_032043.3:c.3700T>C CA400477789 NM_032043.3:c.3702T>G CA400477790 NM_032043.3:c.3702T>A