Allele Registry

Canonical Allele Identifier: PA168228

Gene: BRIP1 HGNC NCBI

ClinVar RCV:

RCV000131481

RCV000460063

RCV000663002

RCV003315907

ClinVar Variation:

142390

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Met100Thr	CA168226 NM_032043.3:c.299T>C