Allele Registry

Canonical Allele Identifier: PA298846

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

180928

ClinVar RCV:

RCV000160326

RCV000205057

RCV000212331

RCV002254684

ClinVar Variation:

182336

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Lys979Glu	CA298844 NM_032043.3:c.2935A>G