Allele Registry

Canonical Allele Identifier: PA2580471903

Gene: BRIP1 HGNC NCBI

ClinVar Variation Id: 1798240

ClinVar RCV Id: RCV002442054

ClinVar Variation Id: 2921331

ClinVar RCV Id: RCV003779418

HGVS (amino-acid)	Matching Registered Transcripts
NP_114432.2:p.Ser990Arg	CA400480638 NM_032043.3:c.2970C>A CA400480639 NM_032043.3:c.2970C>G CA400480645 NM_032043.3:c.2968A>C