Allele Registry

Canonical Allele Identifier: PA658663740

Gene: BRIP1 HGNC NCBI

ClinVar Variation Id: 483213

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ser1026Pro	CA8690402 NM_032043.3:c.3076T>C