Allele Registry

Canonical Allele Identifier: PA658723290

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000581220

RCV000686260

ClinVar Variation:

491414

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ile564Thr	CA292282224 NM_032043.3:c.1691T>C