Allele Registry

Canonical Allele Identifier: PA165063

Gene: BRIP1 HGNC NCBI

ClinVar Allele:

151019

ClinVar RCV:

RCV000129774

RCV000478765

RCV001088100

ClinVar Variation:

141305

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Lys897Glu	CA165061 NM_032043.3:c.2689A>G